Ayunova Pharmaceutical LLP

Product Name:

Gentamicin 0.3% + Dexamethasone 0.1% Cream / Ointment

Description:

Gentamicin + Dexamethasone Cream/Ointment is a combination topical formulation that provides antibacterial and anti-inflammatory action for infected and inflamed skin conditions.

• Gentamicin 0.3% – a broad-spectrum antibiotic effective against Gram-positive and Gram-negative bacteria, helping to treat and prevent bacterial infections.

• Dexamethasone 0.1% – a corticosteroid that reduces inflammation, redness, and itching, providing rapid symptomatic relief.

This combination is ideal for dermatitis, eczema, and other bacterial skin infections with inflammation, offering fast relief and infection control.

Composition:

Each gram contains:

• Gentamicin Sulphate BP/USP – 0.3% w/w

• Dexamethasone BP/USP – 0.1% w/w

• Excipients: Suitable cream or ointment base

Uses / Indications:

• Treatment of bacterial skin infections with inflammation

• Management of eczema, dermatitis, and allergic skin reactions complicated by infection

• Relief from itching, redness, and swelling

• Symptomatic treatment of infected and inflamed skin lesions

Dosage & Administration:

• Apply a thin layer to the affected area 1–2 times daily or as prescribed

• Gently rub until absorbed

• Avoid contact with eyes and mucous membranes

• Use under medical supervision, especially for prolonged therapy

Packaging:

• Tubes: 10 g / 15 g / 20 g / 30 g / 50 g

• Cream or ointment form for easy application

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Product Description

Human Normal Immunoglobulin 50% IP (for intravenous use) is a sterile, purified preparation of human plasma immunoglobulins (IgG) used for passive immunization and immune support. It provides immediate antibody protection against a wide range of infections and is indicated in patients with primary or secondary immunodeficiency. The product is formulated for intravenous administration (IVIG) and meets Indian Pharmacopoeia (IP) standards for purity, safety, and potency.

Composition

Each ml contains:

• Human Normal Immunoglobulin (IgG) 50% w/v IP

• Stabilizers (as per formulation) – q.s.

• Solvent: Water for Injection IP

Uses / Indications

Human Normal Immunoglobulin 50% IP is indicated for:

• Replacement therapy in primary immunodeficiency disorders (e.g., agammaglobulinemia, common variable immunodeficiency)

• Secondary immunodeficiency due to chronic lymphocytic leukemia, bone marrow transplantation, or chemotherapy

• Prevention and treatment of infections in immunocompromised patients

• Autoimmune and inflammatory conditions (as prescribed by a physician)

Dosage & Administration

• Administered by intravenous infusion only, under medical supervision

• Dosage depends on patient weight, clinical condition, and indication

• Infusion should be started slowly and monitored for adverse reactions

Storage Instructions

• Store at 2°C to 8°C (refrigerated)

• Protect from light

• Do not freeze

• Keep out of reach of children

Product Name:

Urea 10% Cream / Ointment

Description:

Urea 10% Cream/Ointment is a topical keratolytic and moisturizing agent widely used for the treatment of dry, rough, and scaly skin conditions. It works by softening and dissolving the keratin in the skin, improving hydration, and promoting smoothness.

The formulation is suitable for managing xerosis, ichthyosis, psoriasis, calluses, and hyperkeratotic skin conditions. Available in cream or ointment form, it provides effective hydration and skin repair.

Composition:

Each gram contains:

• Urea BP/USP – 10% w/w

• Excipients: Suitable cream or ointment base

(Exact composition may vary slightly depending on manufacturer.)

Uses / Indications:

• Treatment of dry and rough skin (xerosis)

• Management of hyperkeratosis and calluses

• Supportive therapy in psoriasis and ichthyosis

• Promotes skin hydration and smoothness

• Softening of thickened or scaly skin

Dosage & Administration:

• Apply a thin layer to the affected area 1–2 times daily

• Gently massage until absorbed

• Avoid contact with eyes and mucous membranes

• Use under medical supervision for prolonged therapy

Packaging:

• Tubes: 10 g / 15 g / 20 g / 30 g / 50 g

• Cream or ointment as per requirement

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from direct sunlight and moisture

• Keep out of reach of children

Product Name:

Diclofenac 1% + Capsaicin 1% Cream / Ointment

Description:

Diclofenac + Capsaicin Cream/Ointment is a dual-action topical formulation designed for pain relief in muscles and joints.

• Diclofenac 1% – a non-steroidal anti-inflammatory drug (NSAID) that reduces inflammation and pain in the affected area.

• Capsaicin 1% – a natural compound that provides warming sensation and reduces pain signals, aiding in relief from chronic pain conditions.

This combination is ideal for arthritis, musculoskeletal pain, sprains, strains, and neuropathic pain, offering fast and long-lasting relief.

Composition:

Each gram contains:

• Diclofenac Sodium BP/USP – 1% w/w

• Capsaicin BP/USP – 1% w/w

• Excipients: Suitable cream or ointment base

Uses / Indications:

• Relief from muscle and joint pain

• Management of arthritis, osteoarthritis, and back pain

• Alleviation of sprains, strains, and soft tissue injuries

• Supportive therapy for chronic neuropathic pain

Dosage & Administration:

• Apply a thin layer to the affected area 2–3 times daily or as directed

• Gently massage until absorbed

• Avoid contact with eyes and mucous membranes

• Wash hands after application

• Use under medical supervision if required for prolonged periods

Packaging:

• Tubes: 30 g / 50 g / 100 g

• Cream or ointment form for easy topical application

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Product Name:

Amoxicillin 500 mg + Clavulanic Acid 125 mg Tablets BP (Total 625 mg)

Description:

Amoxicillin + Clavulanic Acid 625 mg Tablets BP is a broad-spectrum antibiotic combination used for the treatment of bacterial infections.

• Amoxicillin – a β-lactam antibiotic that inhibits bacterial cell wall synthesis, effectively killing susceptible bacteria.

• Clavulanic Acid – a β-lactamase inhibitor that prevents degradation of amoxicillin, extending its activity against β-lactamase-producing bacteria.

This combination is highly effective in respiratory, urinary, skin, soft tissue, and ENT infections, and is commonly used in community and hospital settings.

Composition:

Each tablet contains:

• Amoxicillin Trihydrate BP/USP – 500 mg

• Clavulanic Acid BP/USP – 125 mg

• Excipients: Suitable tablet base, binders, and fillers

Uses / Indications:

Amoxicillin + Clavulanic Acid 625 mg Tablets are indicated for:

1. Respiratory Tract Infections

   • Acute bacterial sinusitis, bronchitis, and pneumonia

2. ENT Infections

   • Otitis media, tonsillitis, pharyngitis

3. Urinary Tract Infections

   • Cystitis, pyelonephritis

4. Skin and Soft Tissue Infections

   • Cellulitis, abscesses, wound infections

5. Dental Infections

   • Periodontal abscess and other oral infections

6. Bone and Joint Infections (in combination with proper therapy)

7. Other β-lactamase-producing bacterial infections

Dosage & Administration:

• Adults: One tablet every 12 hours or as prescribed

• Can be taken with or without food

• Complete the full course to prevent resistance

• Dosage adjustment may be needed in renal impairment

Packaging:

• Blister packs: 10 / 14 / 20 / 28 tablets per strip

• Boxes with product information leaflet

Storage:

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Product Description

Dexmedetomidine Injection USP 100 mcg/ml is a highly selective alpha-2 adrenergic receptor agonist used for sedation and anxiolysis in intensive care and procedural settings. It provides cooperative, arousable sedation with minimal respiratory depression, making it ideal for use in ICUs, operation theatres, and procedural sedation units. The injection is supplied as a clear, colorless sterile solution intended for intravenous use after dilution.

Composition

Each ml contains:

• Dexmedetomidine Hydrochloride USP equivalent to Dexmedetomidine 100 mcg

• Water for Injection USP – q.s.

Uses / Indications

Indicated for:

• Sedation of intubated and mechanically ventilated patients in ICU

• Procedural sedation for diagnostic and surgical procedures

• Sedation of non-intubated patients under monitored anesthesia care

• Adjunct to general anesthesia

Dosage & Administration

• Administered by intravenous infusion after dilution

• Dosage and duration as directed by an anesthesiologist or intensivist

• Continuous monitoring of blood pressure, heart rate, and oxygen saturation is required

Storage Instructions

• Store below 25°C

• Protect from light

• Do not freeze

Packaging

• Ampoule or vial

• Strength: 100 mcg/ml

• Pack size: As per manufacturer

Shelf Life

• As mentioned on the product label

Precautions & Warnings

• For hospital use only

• Prescription medicine

• May cause hypotension and bradycardia

Product Description

Lenalidomide Capsules 10 mg are an immunomodulatory and antineoplastic agent used in the treatment of certain hematological cancers. Lenalidomide works by modulating the immune system, inhibiting tumor cell proliferation, and preventing angiogenesis. The capsules are intended for oral administration and must be used under strict medical supervision, particularly due to its teratogenic potential.

Composition

Each hard gelatin capsule contains:

• Lenalidomide IP – 10 mg

• Excipients – q.s.

Uses / Indications

Lenalidomide Capsules 10 mg are indicated for:

• Multiple myeloma (in combination with dexamethasone or other agents)

• Myelodysplastic syndromes (MDS) with deletion 5q abnormality

• Mantle cell lymphoma (MCL) (relapsed or refractory)

• Follicular lymphoma and marginal zone lymphoma (as prescribed)

Dosage & Administration

• Dosage and treatment cycle as prescribed by the oncologist

• Usually taken once daily for a fixed number of days in a treatment cycle

• Capsules should be swallowed whole with water

• Do not open, crush, or chew the capsules

Storage Instructions

• Store below 25°C

• Protect from moisture and light

• Keep out of reach of children

Packaging

• Blister strips or HDPE bottles

• Strength: 10 mg

• Pack size: As per manufacturer

Product Description

Zoledronic Acid Injection IP 4 mg is a bisphosphonate class medication used to prevent and treat bone-related complications associated with cancer, osteoporosis, and metabolic bone diseases. It works by inhibiting osteoclast-mediated bone resorption, thereby increasing bone mineral density and reducing the risk of fractures. The injection is supplied as a sterile, clear solution for intravenous use under medical supervision.

Composition

Each vial contains:

• Zoledronic Acid IP – 4 mg

• Excipients – q.s.

Uses / Indications

Zoledronic Acid Injection IP 4 mg is indicated for:

• Treatment of osteoporosis in postmenopausal women and men

• Management of bone metastases in cancer patients

• Prevention of skeletal-related events in patients with multiple myeloma or solid tumors

• Treatment of Paget’s disease of bone

• Hypercalcemia of malignancy

Dosage & Administration

• Administered by intravenous infusion as prescribed by the physician

• Dose and frequency depend on indication and patient condition

• Adequate hydration is recommended before administration

Storage Instructions

• Store below 25°C

• Protect from light

• Do not freeze

Packaging

• Single-dose vial

• Strength: 4 mg

APRITANT IV Fosaprepitant Injection 150 mg/Vial Product Description

APRITANT IV is a sterile injectable formulation containing Fosaprepitant, a neurokinin-1 (NK1) receptor antagonist. It is used for the prevention of acute and delayed nausea and vomiting associated with highly and moderately emetogenic cancer chemotherapy. Fosaprepitant is a prodrug of aprepitant and is administered intravenously under medical supervision in hospital or clinical settings.

Composition

• Active Ingredient:
  Fosaprepitant Dimeglumine – equivalent to Fosaprepitant 150 mg

• Excipients:
  q.s.

• Dosage Form:
  Sterile Lyophilized Powder for Injection

Uses / Indications

APRITANT IV is indicated for:

• Prevention of acute and delayed chemotherapy-induced nausea and vomiting (CINV)

• Used as part of combination antiemetic therapy as prescribed by an oncologist

(Prescription medicine – hospital use only)

Dosage & Administration

• Administered as an intravenous infusion

• To be reconstituted and diluted before use

• Dosage and administration schedule as directed by the treating physician

• To be given only by trained healthcare professionals

Storage Instructions

• Store below 25°C

• Protect from light and moisture

• Do not freeze

• Use reconstituted solution within the recommended time

Precautions & Warnings

• For prescription use only

• Hypersensitivity reactions may occur; use under medical supervision

• Use with caution in patients with liver impairment

• Drug interactions should be evaluated before administration

Packaging Details

• Single-dose vial containing 150 mg

• Packed with protective outer carton

Quality Standards

• Manufactured in accordance with GMP guidelines

• Tested for sterility, safety, and potency

Country of Origin

• India

Viraday Tablets – Bottle of 30 Tablets Product Description

Viraday Tablets are a fixed-dose combination antiretroviral medication used in the treatment of HIV-1 infection. It contains Tenofovir Disoproxil Fumarate, Emtricitabine, and Efavirenz, which work together to inhibit viral replication and reduce viral load. Viraday is commonly prescribed as part of first-line antiretroviral therapy (ART) and helps improve immune function when taken regularly under medical supervision.

Composition

Each film-coated tablet contains:

• Tenofovir Disoproxil Fumarate IP – 300 mg

• Emtricitabine IP – 200 mg

• Efavirenz IP – 600 mg

• Excipients – q.s.

Uses / Indications

Viraday Tablets are indicated for:

• Treatment of HIV-1 infection in adults and adolescents

• Part of combination antiretroviral therapy (ART)

• Long-term viral suppression and immune system support

Dosage & Administration

• For oral use only

• Usually one tablet once daily, preferably at bedtime or as directed by a physician

• Can be taken with or without food

• Strict adherence to dosage schedule is essential for effectiveness

Key Features

• Triple-drug fixed dose combination

• Convenient once-daily dosing

• WHO-recommended regimen for HIV treatment

• Suitable for long-term ART management

Storage Instructions

• Store below 30°C

• Protect from moisture and light

• Keep the bottle tightly closed

• Keep out of reach of children

Packaging Details

• Form: Film-coated tablet

• Pack Size: Bottle of 30 tablet

Product Description

Pneumococcal 13-Valent Conjugate Vaccine (PCV-13) is a sterile vaccine designed to provide active immunization against 13 serotypes of Streptococcus pneumoniae. It helps prevent invasive pneumococcal diseases, including pneumonia, meningitis, bacteremia, and otitis media. The vaccine is suitable for infants, children, adults, and elderly patients, especially those at increased risk due to chronic medical conditions.

Composition

Each 0.5 ml dose contains pneumococcal polysaccharides of the following 13 serotypes, individually conjugated to a carrier protein:
1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 23F

Excipients and buffer – q.s.

Uses / Indications

Pneumococcal 13-Valent Conjugate Vaccine is indicated for prevention of:

• Pneumococcal pneumonia

• Invasive pneumococcal disease (IPD)

• Meningitis and bacteremia

• Acute otitis media

Recommended for:

• Infants and children (as per national immunization schedule)

• Adults and elderly (≥50 years)

• Patients with chronic heart, lung, liver, kidney disease, diabetes, or immunocompromised conditions

Dosage & Administration

• Intramuscular injection only

• Dose: 0.5 ml

• Injection site:

  • Infants: anterolateral thigh

  • Adults: deltoid muscle

• Vaccination schedule as per physician advice or immunization guidelines

Storage Instructions

• Store at 2–8°C

• Do not freeze

• Protect from light

• Shake well before use

Packaging

• Single-dose prefilled syringe or vial

• Volume: 0.5 ml

Product Name:

Vitamin D₃ (Cholecalciferol) Pre-Filled Syringe (PFS) 600,000 IU / 1 ml

Description:

Vitamin D₃ (Cholecalciferol) is a fat-soluble vitamin essential for calcium and phosphorus homeostasis and bone health. It helps in the prevention and treatment of vitamin D deficiency, rickets, osteomalacia, and hypocalcemia. The high-dose pre-filled syringe (PFS) formulation ensures precise dosing, sterility, and convenient intramuscular or subcutaneous administration, making it suitable for rapid correction of deficiency in adults and children.

Composition (per 1 ml PFS):

• Vitamin D₃ (Cholecalciferol): 600,000 IU

• Excipients: Oil base (such as arachis oil or medium-chain triglycerides), BP/USP-grade stabilizers

Each pre-filled syringe delivers 600,000 IU of Vitamin D₃ in 1 ml.

Uses / Indications:

• Treatment and prevention of vitamin D deficiency

• Rickets and osteomalacia in children and adults

• Hypocalcemia secondary to vitamin D deficiency

• Supportive therapy for osteoporosis

• Patients unable to take oral supplementation

Dosage and Administration:

• Administered via intramuscular or subcutaneous injection

• Dosage: Single high-dose injection or as prescribed by a physician

• Must be used under the supervision of a qualified healthcare professional

Key Features:

• High-dose Vitamin D₃ for rapid correction of deficiency

• Pre-filled syringe ensures accurate, ready-to-use dosing

• Sterile, pyrogen-free, and BP/USP-compliant formulation

• Supports bone health, calcium absorption, and metabolic functions

Packaging:

• 1 ml PFS containing 600,000 IU Vitamin D₃

• Supplied in individual sterile packs or cartons

Storage Conditions:

• Store at 2–8°C (refrigerated)

• Protect from light

• Keep out of reach of children

Product Name:

Tretinoin 0.025% Cream / Ointment

Description:

Tretinoin 0.025% Cream/Ointment is a topical retinoid used in the treatment of acne vulgaris, fine wrinkles, and hyperpigmentation. It works by modulating skin cell turnover, promoting exfoliation of dead skin cells, and preventing the formation of comedones, leading to clearer, smoother skin.

This formulation is widely used in dermatology clinics and cosmetic therapy for anti-aging and acne management.

Composition:

Each gram contains:

• Tretinoin BP/USP – 0.025% w/w

• Excipients: Suitable cream or ointment base

(Exact composition may vary slightly depending on manufacturer.)

Uses / Indications:

• Treatment of acne vulgaris

• Management of fine wrinkles and photo-damaged skin

• Treatment of hyperpigmentation and dark spots

• Improves skin texture and smoothness

• Promotes healthy skin renewal

Dosage & Administration:

• Apply a thin layer to the affected area once daily at night

• Avoid contact with eyes, lips, and mucous membranes

• Use sunscreen during the day to prevent photosensitivity

• Use under medical supervision, especially in sensitive skin

Packaging:

• Tubes: 10 g / 15 g / 20 g / 30 g

• Cream or ointment form as per requirement

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Product Name:

Mometasone Furoate 0.1% Cream / Ointment

Description:

Mometasone Furoate 0.1% Cream/Ointment is a potent topical corticosteroid used to relieve inflammation, itching, and redness associated with various dermatological conditions. It provides effective symptomatic relief in conditions such as eczema, psoriasis, dermatitis, and allergic skin reactions.

The cream and ointment formulations allow flexible application depending on skin type and affected area, making it suitable for both hospital and outpatient use.

Composition:

Each gram contains:

• Mometasone Furoate BP/USP – 0.1% w/w

• Excipients: Suitable cream or ointment base

(Exact composition may vary slightly depending on manufacturer.)

Uses / Indications:

• Inflammatory skin conditions such as eczema and dermatitis

• Management of psoriasis and lichen planus

• Relief from itching, swelling, and redness due to allergic reactions

• Symptomatic treatment of pruritic skin conditions

Dosage & Administration:

• Apply a thin layer to the affected area once or twice daily as prescribed

• Gently rub until absorbed

• Avoid contact with eyes and mucous membranes

• Use under medical supervision for prolonged periods

Packaging:

• Tubes: 10 g / 15 g / 20 g / 30 g

• Cream or ointment form as per requirement

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from direct sunlight and moisture

• Keep out of reach of children

Product Name:

Hydrocortisone 1% Cream / Ointment

Description:

Hydrocortisone 1% Cream/Ointment is a mild topical corticosteroid used to relieve inflammation, redness, itching, and swelling associated with various dermatological conditions. It provides effective symptomatic relief for eczema, dermatitis, insect bites, rashes, and allergic skin reactions.

Available in both cream and ointment forms, it is suitable for hospital, clinic, and home use, ensuring flexibility depending on skin type and affected area.

Composition:

Each gram contains:

• Hydrocortisone BP/USP – 1% w/w

• Excipients: Suitable cream or ointment base

(Exact composition may vary slightly depending on manufacturer.)

Uses / Indications:

• Treatment of eczema and dermatitis

• Relief from itching, redness, and swelling

• Management of allergic skin reactions and insect bites

• Symptomatic treatment of pruritic skin conditions

Dosage & Administration:

• Apply a thin layer to the affected area 1–2 times daily

• Gently rub until absorbed

• Avoid contact with eyes and mucous membranes

• Use under medical supervision for prolonged therapy

Packaging:

• Tubes: 10 g / 15 g / 20 g / 30 g / 50 g

• Cream or ointment form as per requirement

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from direct sunlight and moisture

• Keep out of reach of children

Product Name:

Teriparatide Pre-Filled Syringe (PFS) 20 mcg / 0.8 ml

Description:

Teriparatide is a recombinant form of human parathyroid hormone (PTH 1-34) used in the treatment of osteoporosis. It stimulates new bone formation by activating osteoblasts, increasing bone mineral density, and reducing the risk of fractures in patients with severe osteoporosis. The pre-filled syringe (PFS) ensures accurate dosing, sterile administration, and convenient subcutaneous delivery for home or clinical use.

Composition (per 0.8 ml PFS):

• Teriparatide: 20 mcg

• Excipients: Buffer solution, stabilizers, and BP/USP-grade excipients

Each pre-filled syringe delivers 20 mcg of Teriparatide in 0.8 ml for subcutaneous injection.

Uses / Indications:

• Treatment of osteoporosis in postmenopausal women at high risk of fracture

• Treatment of osteoporosis in men at high risk of fracture

• Glucocorticoid-induced osteoporosis in men and women

• Patients who cannot tolerate or respond to other osteoporosis therapies

Dosage and Administration:

• Administered via subcutaneous injection once daily

• Typical dose: 20 mcg daily, at any time of the day, in the thigh or abdominal area

• Must be used under the supervision of a qualified healthcare professional

Key Features:

• Stimulates bone formation and increases bone mineral density

• Pre-filled syringe for accurate, ready-to-use dosing

• Sterile, BP/USP-compliant formulation

• Suitable for home administration under medical guidance

Packaging:

• 0.8 ml PFS containing 20 mcg Teriparatide

• Supplied in individual sterile packs or cartons

Storage Conditions:

• Store at 2–8°C (refrigerated)

• Protect from light

• Do not freeze

• Keep out of reach of children

Product Name:

Beclomethasone 0.025% + Neomycin 0.5% + Clotrimazole 1% Cream / Ointment

Description:

Beclomethasone + Neomycin + Clotrimazole Cream/Ointment is a triple-action topical formulation combining anti-inflammatory, antibacterial, and antifungal properties.

• Beclomethasone 0.025% – a corticosteroid that reduces inflammation, redness, and itching.

• Neomycin 0.5% – a topical antibiotic effective against Gram-positive bacterial infections, preventing or treating secondary bacterial infections.

• Clotrimazole 1% – a broad-spectrum antifungal effective against dermatophytes, yeasts, and Candida species, managing fungal infections.

This combination is suitable for infected inflammatory skin conditions, providing rapid relief, infection control, and comprehensive skin care.

Composition:

Each gram contains:

• Beclomethasone BP/USP – 0.025% w/w

• Neomycin Sulphate BP/USP – 0.5% w/w

• Clotrimazole BP/USP – 1% w/w

• Excipients: Suitable cream or ointment base

Uses / Indications:

• Inflammatory skin conditions with secondary bacterial and fungal infections

• Management of eczema, dermatitis, psoriasis, tinea, and candidiasis complicated by infection

• Relief from itching, redness, scaling, and bacterial/fungal colonization

• Symptomatic treatment of pruritic and infected skin lesions

Dosage & Administration:

• Apply a thin layer to the affected area 1–2 times daily as prescribed

• Gently rub until absorbed

• Avoid contact with eyes and mucous membranes

• Use under medical supervision, especially for prolonged therapy

Packaging:

• Tubes: 10 g / 15 g / 20 g / 30 g / 50 g

• Cream or ointment form as per requirement

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Product Name:

Diclofenac Diethylamine 1% Gel

Description:

Diclofenac Diethylamine 1% Gel is a topical non-steroidal anti-inflammatory drug (NSAID) used for pain relief and reduction of inflammation in musculoskeletal conditions. It works by inhibiting prostaglandin synthesis, thereby reducing pain, swelling, and stiffness.

This gel is commonly used for joint pain, muscle strains, sprains, and sports injuries. Its topical application ensures targeted action with minimal systemic side effects.

Composition:

Each gram contains:

• Diclofenac Diethylamine BP/USP – 1% w/w

• Excipients: Suitable gel base

Uses / Indications:

• Relief of pain and inflammation in joints and muscles

• Treatment of sprains, strains, and sports injuries

• Management of osteoarthritis and rheumatoid arthritis pain

• Reduces swelling, stiffness, and localized pain

Dosage & Administration:

• Apply a thin layer to the affected area 2–3 times daily

• Gently massage until absorbed

• Avoid contact with eyes and mucous membranes

• Wash hands after application

• Use as directed by a healthcare professional

Packaging:

• Tubes: 15 g / 30 g / 50 g / 100 g

• Gel form for easy topical application

• Box packaging with product information leaflet

Storage:

• Store below 25°C

• Protect from direct sunlight and moisture

• Keep out of reach of children

Product Name:

Epinephrine (Adrenaline) Auto-Injector PFS 0.3 mg / 0.3 ml

Description:

Epinephrine Auto-Injector is a fast-acting emergency device used for the treatment of severe allergic reactions (anaphylaxis). Epinephrine, a potent sympathomimetic, stimulates alpha and beta-adrenergic receptors, resulting in vasoconstriction, bronchodilation, and increased cardiac output. The auto-injector provides a pre-measured, ready-to-use dose for rapid intramuscular administration, ensuring timely intervention in life-threatening allergic emergencies.

Composition (per 0.3 ml PFS):

• Epinephrine (Adrenaline): 0.3 mg

• Excipients: Sodium chloride, water for injection, and BP/USP-grade stabilizers

Each auto-injector delivers 0.3 mg of epinephrine in 0.3 ml intramuscularly.

Uses / Indications:

• Emergency treatment of anaphylaxis caused by:

  • Food allergies

  • Insect stings or bites

  • Drug hypersensitivity

• Severe asthma attacks unresponsive to standard therapy

• Rapid relief of acute allergic symptoms in emergency situations

Dosage and Administration:

• Administered intramuscularly, preferably into the outer thigh

• Single-use auto-injector provides a precise emergency dose

• Repeat dose may be administered after 5–15 minutes if symptoms persist

• Always use under medical supervision or in an emergency

Key Features:

• Pre-measured, ready-to-use auto-injector for emergencies

• Rapid onset of action to prevent progression of anaphylaxis

• Sterile, BP/USP-compliant formulation

• Portable and convenient for home, travel, or outdoor use

Packaging:

• 0.3 ml auto-injector containing 0.3 mg Epinephrine

• Supplied in individual sterile packs with protective casing

Storage Conditions:

• Store at 20–25°C (room temperature), protect from light

• Do not freeze

Product Name

Risperidone Tablets BP – 1 mg

Product Description

Risperidone Tablets BP is an atypical antipsychotic used for the management of schizophrenia, bipolar disorder, and irritability associated with autism. It works by modulating dopamine and serotonin receptors in the brain, helping to reduce hallucinations, delusions, aggression, and mood swings.

These tablets are widely prescribed in psychiatric clinics, hospitals, and mental health centers for both acute and maintenance therapy in psychotic and mood disorders.

Composition

Each tablet contains:

• Risperidone BP – 1 mg

• Excipients: q.s. to make a tablet

Major Indications / Uses Primary Indications

• Schizophrenia – treatment of acute and chronic episodes

• Bipolar disorder – management of mania or mixed episodes

• Autism spectrum disorder – for irritability, aggression, and mood swings

Other Uses

• Adjunct therapy in treatment-resistant depression

• Behavioral disturbances in dementia (off-label use under supervision)

• Management of psychotic symptoms in other psychiatric conditions

Dosage & Administration

• Route: Oral

• Typical Adult Dose: 1–6 mg/day, divided or single dose, depending on clinical response

• Pediatric Dose: Only under specialist guidance

• Monitoring: Mental status, extrapyramidal symptoms, weight, blood sugar, and lipid profile

⚠ Administer under medical supervision
⚠ Avoid abrupt discontinuation; tapering may be required

Packaging Details

• Strip packaging: 10 × 10 tablets

• Bottle packaging: 100 tablets per bottle

• Hospital and bulk packaging available

Storage Conditions

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Product Description

Pneumococcal 20-Valent Conjugate Vaccine (PCV-20) is a sterile conjugate vaccine that provides active immunization against 20 serotypes of Streptococcus pneumoniae. It is designed to protect against invasive pneumococcal disease (IPD) and pneumonia, offering broader serotype coverage compared to earlier conjugate vaccines. PCV-20 is primarily recommended for adults and elderly individuals, especially those with underlying medical conditions or increased risk of pneumococcal infection.

Composition

Each 0.5 ml dose contains pneumococcal polysaccharides of the following 20 serotypes, individually conjugated to a carrier protein:

1, 3, 4, 5, 6A, 6B, 7F, 8, 9V, 10A, 11A, 12F, 14, 15B, 18C, 19A, 19F, 22F, 23F, 33F

Excipients and buffer – q.s.

Uses / Indications

Pneumococcal 20-Valent Conjugate Vaccine is indicated for prevention of:

• Invasive pneumococcal disease (IPD)

• Pneumococcal pneumonia

• Bacteremia and meningitis caused by vaccine serotypes

Recommended for:

• Adults ≥18 years

• Elderly patients

• Individuals with chronic heart, lung, liver, kidney disease, diabetes

• Immunocompromised patients and smokers (as per physician advice)

Dosage & Administration

• Intramuscular injection only

• Dose: 0.5 ml

• Injection site: Deltoid muscle

• Vaccination schedule as per national guidelines or physician recommendation

Storage Instructions

• Store at 2–8°C

• Do not freeze

• Protect from light

• Maintain cold-chain during storage and transportation

Packaging

• Single-dose prefilled syringe or vial

• Volume: 0.5 ml

Product Description

Progesterone Vaginal Gel E.P. 8% is a hormonal preparation containing natural progesterone used for assisted reproductive technology (ART), luteal phase support, and management of gynecological conditions. The vaginal gel ensures localized delivery, improved absorption, and effective hormonal support. It is widely used to support early pregnancy, regulate menstrual cycles, and improve implantation rates in fertility treatments.

Composition

Each gram of vaginal gel contains:

• Progesterone E.P. / USP – 80 mg (8%)

• Suitable bioadhesive gel base – q.s.

• Excipients – q.s.

Uses / Indications

Progesterone Vaginal Gel E.P. 8% is indicated for:

• Luteal phase support in ART protocols (IVF, ICSI)

• Prevention of threatened miscarriage in early pregnancy

• Amenorrhea or irregular menstruation

• Hormone replacement therapy (HRT) in postmenopausal women

• Other gynecological conditions requiring progesterone supplementation

Dosage & Administration

• Administered intravaginally, usually once or twice daily as prescribed by the physician

• Dose and duration depend on clinical indication and ART protocol

• Apply using the applicator provided for accurate dosing

• Maintain hygiene during administration

Storage Instructions

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Packaging

• Vaginal gel tube

• Strength: 8% (80 mg/g)

• Pack size: As per manufacturer (commonly 45 g or 90 g tubes)

GINETTE 35 – Oral Contraceptive Tablet Product Description

GINETTE 35 Tablet is a combined oral contraceptive containing Ethinylestradiol and Desogestrel. It is used for the prevention of pregnancy and for regulating menstrual cycles. The tablet works by inhibiting ovulation, altering the cervical mucus, and changing the endometrial lining, thereby reducing the chances of conception.

Composition

Each film-coated tablet contains:

• Ethinylestradiol IP – 35 mcg

• Desogestrel IP – 0.15 mg

• Excipients – q.s.

• Dosage Form: Film-coated tablet

Uses / Indications

GINETTE 35 Tablets are indicated for:

• Contraception (prevention of pregnancy)

• Regulation of menstrual cycles

• Treatment of menstrual disorders such as dysmenorrhea

• Reduction of acne in women (as per physician recommendation)

Dosage & Administration

• For oral use only

• One tablet daily at the same time each day, preferably after a meal

• Start on the first day of menstruation or as directed by a physician

• Continue as prescribed for maximum effectiveness

Key Features

• Combined estrogen-progestin contraceptive

• Highly effective in preventing pregnancy

• Helps regulate menstrual cycles

• Suitable for long-term use under medical supervision

Storage Instructions

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Product Description

PROPESS 10 mg Vaginal Insert is a prostaglandin E2 (PGE2) controlled-release insert used for cervical ripening and induction of labor in pregnant women at or near term. The insert releases dinoprostone gradually to soften the cervix and stimulate uterine contractions, facilitating a safer and more effective induction of labor. PROPESS is intended for vaginal administration under medical supervision.

Composition

Each vaginal insert contains:

• Dinoprostone IP / USP (Prostaglandin E2) – 10 mg

• Controlled-release hydrogel matrix – q.s.

• Excipients – q.s.

Uses / Indications

PROPESS 10 mg Vaginal Inserts are indicated for:

• Cervical ripening in women at or near term (≥37 weeks of gestation)

• Labor induction in cases where vaginal delivery is medically indicated

• Helps achieve favorable cervical conditions for safe labor

• Used under strict medical supervision in hospital or clinical settings

Dosage & Administration

• Single vaginal insert (10 mg) is inserted high into the posterior fornix of the vagina by a trained healthcare professional

• Duration: Up to 24 hours, or until labor begins

• Continuous maternal and fetal monitoring is recommended during use

• Remove the insert if active labor is established or adverse effects occur

Storage Instructions

• Store 2–8°C, protected from light

• Do not freeze

• Keep out of reach of children

Packaging

• Pack of 5 vaginal inserts

• Strength: 10 mg per insert

CEREBROGEN – Cerebroprotein Hydrolysate for Injection 60 mg Product Description

CEREBROGEN Injection contains Cerebroprotein Hydrolysate, a neurotrophic agent used to support brain metabolism and neuronal function. It is commonly prescribed in neurological conditions associated with cognitive impairment and cerebrovascular disorders. The injection is supplied as a sterile, ready-to-use solution for intramuscular or intravenous administration under medical supervision.

Composition

Each ampoule/vial contains:

• Cerebroprotein Hydrolysate – 60 mg

• Water for Injection – q.s.

• Dosage Form: Injection

Uses / Indications

CEREBROGEN Injection is indicated for supportive treatment in:

• Cerebrovascular disorders

• Ischemic stroke (adjunct therapy)

• Traumatic brain injury

• Dementia and Alzheimer’s disease

• Cognitive impairment

• Neurodegenerative disorders

Dosage & Administration

• Administered by IM or IV route

• Dosage and duration as directed by a registered medical practitioner

• To be used under strict medical supervision

Key Features

• Neurotrophic and neuroprotective agent

• Supports neuronal repair and brain metabolism

• Used in neurological and cognitive disorders

• Suitable for hospital and clinical use

Storage Instructions

• Store below 25°C

• Protect from light

• Do not freeze

• Keep out of reach of children

DANOGEN – Danazol Capsules IP 200 mg Product Description

DANOGEN Capsules contain Danazol, a synthetic steroid with antigonadotropic and androgenic properties. It is primarily used in the management of endometriosis, fibrocystic breast disease, and hereditary angioedema. Danazol works by suppressing pituitary gonadotropins, leading to reduced estrogen production. The capsules are intended for oral administration under medical supervision.

Composition

Each hard gelatin capsule contains:

• Danazol IP – 200 mg

• Excipients – q.s.

• Dosage Form: Capsule

Uses / Indications

DANOGEN Capsules are indicated for the treatment of:

• Endometriosis

• Fibrocystic breast disease

• Hereditary angioedema (prevention of attacks)

• Certain hormone-related disorders as prescribed by a physician

Dosage & Administration

• For oral use only

• Dosage and duration to be determined by a registered medical practitioner

• To be taken as advised, preferably at the same time each day

Key Features

• Antigonadotropic synthetic steroid

• Effective in hormone-dependent conditions

• IP-grade formulation

• Suitable for long-term therapy under supervision

Storage Instructions

• Store below 25°C

• Protect from light and moisture

• Keep out of reach of children

Cisatracurium Besylate Injection 20 mg/10 ml Product Description

Cisatracurium Besylate Injection 20 mg/10 ml is a sterile, non-depolarizing neuromuscular blocking agent used to induce skeletal muscle relaxation during surgical procedures or mechanical ventilation. It acts by inhibiting acetylcholine at the neuromuscular junction, providing controlled muscle relaxation. This injection is intended for intravenous use under the supervision of trained healthcare professionals in hospital and clinical settings.

Composition

• Active Ingredient:
  Cisatracurium Besylate – 20 mg / 10 ml

• Excipients:
  q.s.

• Dosage Form:
  Sterile injection

Uses / Indications

Cisatracurium Besylate Injection is indicated for:

• Muscle relaxation during surgery requiring general anesthesia

• Facilitation of endotracheal intubation

• Mechanical ventilation in critical care settings

• As prescribed by an anesthesiologist

(Prescription medicine – hospital and clinical use only)

Dosage & Administration

• Administered intravenously by trained healthcare professionals

• Dosage depends on patient age, weight, and clinical condition

• Monitor neuromuscular function and vital signs during administration

Storage Instructions

• Store below 25°C

• Protect from light

• Keep out of reach of children

• Do not freeze

Precautions & Warnings

• For prescription use only

• Use with caution in patients with liver, kidney, or neuromuscular disorders

• Monitor respiratory and cardiovascular status during administration

• Not recommended during pregnancy unless clearly indicated

Packaging Details

• 10 ml vial containing 20 mg

• Supplied with protective outer carton

Quality Standards

• Manufactured in compliance with IP and GMP guidelines

• Tested for sterility, potency, and safety

Country of Origin

• India

Product Name:

Vitamin C (Ascorbic Acid) High-Dose Pre-Filled Syringe (PFS) 1 g / 5 ml

Description:

Vitamin C (Ascorbic Acid) is a water-soluble vitamin with potent antioxidant properties. High-dose injectable Vitamin C is used for rapid supplementation in patients with deficiency, for immune support, wound healing, and as adjunct therapy in certain clinical conditions. The pre-filled syringe (PFS) ensures accurate dosing, sterility, and convenient intravenous or intramuscular administration.

Composition (per 5 ml PFS):

• Vitamin C (Ascorbic Acid): 1 g

• Excipients: Water for injection, BP/USP-grade stabilizers

Each pre-filled syringe delivers 1 g of Vitamin C in 5 ml solution.

Uses / Indications:

• Treatment and prevention of Vitamin C deficiency (scurvy)

• Supportive therapy for immune system enhancement

• Acceleration of wound healing and tissue repair

• Adjunctive therapy in critically ill or malnourished patients

• High-dose therapy in selected clinical conditions under physician supervision

Dosage and Administration:

• Administered via intravenous or intramuscular injection

• Dosage depends on patient’s clinical condition, age, and physician’s prescription

• Must be used under supervision of a qualified healthcare professional

Key Features:

• High-dose Vitamin C for rapid therapeutic effect

• Pre-filled syringe ensures precise, ready-to-use dosing

• Sterile, pyrogen-free, and BP/USP-compliant formulation

• Supports antioxidant defense, immune health, and tissue repair

Packaging:

• 5 ml PFS containing 1 g Vitamin C

• Supplied in individual sterile packs or cartons

Storage Conditions:

• Store at 2–8°C (refrigerated)

• Protect from light

• Keep out of reach of children