Ayunova Pharmaceutical LLP

Paracetamol For Injection BP is a sterile, clear solution used for the management of fever and mild to moderate pain. It provides rapid analgesic and antipyretic effects and is widely used in hospitals, clinics, and emergency care where oral administration is not feasible. Manufactured according to British Pharmacopoeia (BP) standards, ensuring safe, effective, and high-quality use.

Each 1 ml contains:

• Paracetamol BP – 10 mg / 50 mg / 100 mg (strength may vary)

• Sodium Metabisulphite IP – as antioxidant

• Water for Injection IP – q.s.

• Relief of mild to moderate pain

• Fever management

• Postoperative pain relief

• Pain associated with musculoskeletal or inflammatory conditions

• Administered intravenously (IV)

• Dosage and duration as prescribed by a qualified healthcare professional

• For hospital use only

• Rapid onset of analgesic and antipyretic action

• Sterile, BP-grade quality

• Suitable for patients unable to take oral medication

• Widely used in emergency, ICU, and hospital care

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Pantoprazole For Injection BP is a sterile, clear solution of a proton pump inhibitor (PPI) used to suppress gastric acid secretion. It is ideal for patients who cannot take oral medication and is commonly used in hospital and critical care settings. Pantoprazole works by inhibiting the H⁺/K⁺-ATPase enzyme system in gastric parietal cells, providing effective management of acid-related gastrointestinal disorders. Manufactured in compliance with British Pharmacopoeia (BP) standards.

Each vial contains:

• Pantoprazole Sodium BP – 40 mg / 80 mg (strength may vary)

• Sodium Hydroxide IP – for pH adjustment

• Water for Injection IP – q.s.

(Supplied as powder for reconstitution or ready-to-use solution depending on the pack)

• Treatment of peptic ulcer disease

• Gastroesophageal reflux disease (GERD)

• Zollinger–Ellison syndrome

• Prevention and treatment of stress-related mucosal bleeding

• Acid suppression in critically ill patients

• Administered intravenously (IV) after proper reconstitution

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Rapid and effective gastric acid suppression

• BP-grade sterile formulation

• Suitable for patients unable to take oral medication

• Widely used in ICU, emergency, and gastroenterology care

• Store in a cool, dry place, protected from light

• Use reconstituted solution promptly

• Keep out of reach of children

• Supplied in vials with or without diluent

• Multiple pack sizes available

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Palonosetron For Injection BP is a sterile, clear solution used as a selective 5-HT₃ receptor antagonist to prevent and treat nausea and vomiting associated with chemotherapy, radiotherapy, and postoperative procedures. It provides long-acting antiemetic protection by blocking serotonin receptors in the central nervous system and gastrointestinal tract. Manufactured according to British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and effective hospital use.

Each 1 ml contains:

• Palonosetron Hydrochloride BP – 0.25 mg

• Sodium Chloride IP – q.s.

• Water for Injection IP – q.s.

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

• Prevention of radiotherapy-induced nausea and vomiting (RINV)

• Management of postoperative nausea and vomiting (PONV)

• Anti-emetic support in hospital and clinical settings

• Administered intravenously (IV)

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Long-acting, highly effective anti-emetic injection

• BP-grade sterile formulation

• Rapid onset of action

• Widely used in oncology, surgery, and ICU care

• Store in a cool, dry place

• Protect from light

• Do not freeze

• Supplied in ampoules or vials

• Various pack sizes available

• Tamper-evident, secure packaging

• 24–36 months, as per label

Ondansetron For Injection BP is a sterile, clear solution used as a selective 5-HT₃ receptor antagonist to prevent and treat nausea and vomiting associated with chemotherapy, radiotherapy, and postoperative care. It acts by blocking serotonin receptors in the central nervous system and gastrointestinal tract. Manufactured in compliance with British Pharmacopoeia (BP) standards, ensuring safety, efficacy, and high-quality pharmaceutical standards.

Each 1 ml contains:

• Ondansetron Hydrochloride BP – 2 mg / 4 mg (strength may vary)

• Sodium Chloride IP – q.s.

• Water for Injection IP – q.s.

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

• Prevention of radiotherapy-induced nausea and vomiting (RINV)

• Management of postoperative nausea and vomiting (PONV)

• Anti-emetic support in hospital and clinical settings

• Administered intravenously (IV)

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Highly effective anti-emetic injection

• BP-grade sterile formulation

• Rapid onset of action

• Widely used in oncology, surgery, and ICU care

• Store in a cool, dry place

• Protect from light

• Do not freeze

• Supplied in ampoules or vials

• Various pack sizes available

• Secure, tamper-evident packaging

• 24–36 months, as per label

Rabeprazole For Injection BP is a sterile formulation of a proton pump inhibitor (PPI) used to suppress gastric acid secretion. It is ideal for patients who cannot take oral medication and is commonly used in hospital and critical care settings. Rabeprazole works by inhibiting the H⁺/K⁺-ATPase enzyme system in gastric parietal cells, providing effective management of acid-related gastrointestinal disorders. Manufactured in compliance with British Pharmacopoeia (BP) standards.

Each vial contains:

• Rabeprazole Sodium BP – 20 mg / 40 mg (strength may vary)

• Sodium Hydroxide IP – for pH adjustment

• Water for Injection IP – q.s.

(Supplied as powder for reconstitution or ready-to-use solution depending on the pack)

• Treatment of peptic ulcer disease

• Gastroesophageal reflux disease (GERD)

• Zollinger–Ellison syndrome

• Prevention and treatment of stress-related mucosal bleeding

• Acid suppression in critically ill patients

• Administered intravenously (IV) after proper reconstitution

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Rapid and effective gastric acid suppression

• BP-grade sterile formulation

• Suitable for patients unable to take oral medication

• Widely used in ICU, emergency, and gastroenterology care

• Store in a cool, dry place, protected from light

• Use reconstituted solution promptly

• Keep out of reach of children

• Supplied in vials with or without diluent

• Multiple pack sizes available

• Tamper-evident, secure packaging

• 24–36 months, as per label

Omeprazole For Injection BP is a sterile formulation of a proton pump inhibitor (PPI) used to reduce gastric acid secretion. It is commonly administered in hospital and critical care settings when oral therapy is not feasible. Omeprazole works by inhibiting the gastric H⁺/K⁺-ATPase enzyme system, providing effective management of acid-related gastrointestinal disorders. Manufactured in accordance with British Pharmacopoeia (BP) standards.

Each vial contains:

• Omeprazole BP – 40 mg

• Sodium Hydroxide IP – for pH adjustment

• Water for Injection IP – q.s.

(Supplied as powder with solvent or ready-to-use vial, depending on pack)

• Management of peptic ulcer disease

• Gastroesophageal reflux disease (GERD)

• Zollinger–Ellison syndrome

• Prevention and treatment of stress-related mucosal bleeding

• Acid suppression in critically ill patients

• Administered intravenously (IV) after reconstitution

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Powerful gastric acid suppression

• BP grade sterile formulation

• Suitable for patients unable to take oral medication

• Widely used in ICU, emergency, and gastroenterology care

• Store in a cool, dry place

• Protect from light

• Reconstituted solution should be used promptly

• Supplied in vials with or without diluent

• Various pack sizes available

• Secure and tamper-evident packaging

• 24–36 months, as stated on the label

Ketorolac Tromethamine Injection BP is a sterile, clear solution belonging to the non-steroidal anti-inflammatory drug (NSAID) class. It is used for the short-term management of moderate to severe acute pain, especially in postoperative and emergency settings. The drug works by inhibiting prostaglandin synthesis, providing effective analgesic and anti-inflammatory action. Manufactured in accordance with British Pharmacopoeia (BP) standards for hospital and clinical use.

Each 1 ml contains:

• Ketorolac Tromethamine BP – 30 mg (strength may vary)

• Sodium Chloride IP – q.s.

• Water for Injection IP – q.s.

• Short-term treatment of moderate to severe pain

• Postoperative pain management

• Pain associated with musculoskeletal conditions

• Acute pain relief in emergency and hospital care

• Administered intramuscularly (IM) or intravenously (IV)

• Dosage and duration as prescribed by a qualified healthcare professional

• For hospital use only

• Rapid onset of analgesic effect

• BP grade sterile formulation

• Effective alternative to opioid analgesics

• Widely used in hospitals, ICUs, and emergency departments

• Store in a cool, dry place

• Protect from light

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes available

• Secure and tamper-evident packaging

• 24–36 months, as per label

Granisetron For Injection BP is a sterile, clear solution used as a selective 5-HT₃ receptor antagonist for the prevention and treatment of nausea and vomiting associated with chemotherapy, radiotherapy, and postoperative procedures. It works by blocking serotonin receptors in the central nervous system and gastrointestinal tract. Manufactured in compliance with British Pharmacopoeia (BP) standards for reliable hospital use.

Each 1 ml contains:

• Granisetron Hydrochloride BP – equivalent to 1 mg Granisetron (strength may vary)

• Sodium Chloride IP – q.s.

• Water for Injection IP – q.s.

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

• Prevention of radiotherapy-induced nausea and vomiting

• Management of postoperative nausea and vomiting (PONV)

• Anti-emetic support in hospital and clinical settings

• Administered intravenously (IV)

• Dosage as directed by a qualified healthcare professional

• For hospital use only

• Highly effective anti-emetic injection

• BP grade sterile formulation

• Well tolerated with rapid onset of action

• Widely used in oncology, surgery, and ICU care

• Store in a cool, dry place

• Protect from light

• Do not freeze

• Supplied in ampoules or vials

• Various pack sizes available

• Secure, tamper-evident packaging

• 24–36 months, as stated on the label

Diclofenac Sodium For Injection BP is a sterile, clear solution belonging to the non-steroidal anti-inflammatory drug (NSAID) class. It is widely used for the rapid relief of acute pain, inflammation, and fever. By inhibiting prostaglandin synthesis, it provides effective analgesic and anti-inflammatory action. Manufactured as per British Pharmacopoeia (BP) standards for hospital and clinical use.

Each 1 ml contains:

• Diclofenac Sodium BP – 25 mg / 50 mg (strength may vary)

• Benzyl Alcohol IP – as preservative (where applicable)

• Water for Injection IP – q.s.

• Management of acute and moderate to severe pain

• Postoperative pain relief

• Pain due to musculoskeletal disorders

• Inflammatory conditions

• Fever associated with pain and inflammation

• Administered intramuscularly (IM) or intravenously (IV)

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Fast-acting analgesic and anti-inflammatory effect

• BP grade sterile formulation

• Widely used in hospitals, clinics, and emergency care

• Reliable and effective pain management solution

• Store in a cool, dry place

• Protect from light

• Do not freeze

• Available in ampoules or vials

• Various pack sizes available

• Secure and tamper-evident packaging

• 24–36 months, as per label

Dexamethasone For Injection BP is a sterile, clear solution of a synthetic corticosteroid used for its anti-inflammatory, immunosuppressive, and anti-allergic properties. It is widely used in emergency, ICU, and hospital settings to manage severe inflammatory conditions, allergic reactions, and certain endocrine disorders. Manufactured according to British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and reliable pharmaceutical use.

Each 1 ml contains:

• Dexamethasone Sodium Phosphate BP – 4 mg / 8 mg (strength may vary)

• Sodium Chloride IP – q.s.

• Water for Injection IP – q.s.

• Treatment of severe allergies and anaphylaxis

• Management of inflammatory and autoimmune conditions

• Adjunct therapy in shock and critical care

• Anti-inflammatory therapy in dermatological and respiratory disorders

• Hormonal and endocrine support in certain medical conditions

• Administered intravenously (IV) or intramuscularly (IM)

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Rapid and potent anti-inflammatory effect

• BP-grade sterile formulation

• Widely used in emergency, ICU, and hospital care

• Reliable immunosuppressive and anti-allergic properties

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label

Methylprednisolone For Injection BP is a sterile, clear solution of a synthetic corticosteroid with anti-inflammatory, immunosuppressive, and anti-allergic properties. It is widely used in emergency, ICU, and hospital settings to manage severe inflammatory conditions, allergic reactions, and autoimmune disorders. Manufactured according to British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and reliable pharmaceutical use.

Each 1 ml contains:

• Methylprednisolone Sodium Succinate BP – 40 mg / 125 mg (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Treatment of severe allergies and anaphylaxis

• Management of inflammatory and autoimmune disorders

• Adjunct therapy in shock and critical care

• Anti-inflammatory therapy in dermatological, respiratory, and musculoskeletal conditions

• Hormonal and endocrine support in specific medical conditions

• Administered intravenously (IV) or intramuscularly (IM)

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Rapid and potent anti-inflammatory effect

• BP-grade sterile formulation

• Widely used in emergency, ICU, and hospital care

• Reliable immunosuppressive and anti-allergic properties

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Adrenaline For Injection BP is a sterile, clear solution of a catecholamine used in emergency medicine for its cardiovascular and bronchodilator effects. It is commonly used to treat anaphylaxis, cardiac arrest, and severe asthma attacks. Manufactured in compliance with British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and effective hospital use.

Each 1 ml contains:

• Adrenaline (Epinephrine) BP – 1 mg / ml (1:1000) (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Emergency treatment of anaphylactic reactions

• Management of cardiac arrest and shock

• Treatment of severe asthma attacks

• Supportive therapy in emergency and critical care

• Administered intramuscularly (IM), subcutaneously (SC), or intravenously (IV) as per requirement

• Dosage as prescribed by a qualified healthcare professional

• For hospital and emergency use only

• Rapid onset of action

• BP-grade sterile formulation

• Widely used in ICU, emergency, and hospital care

• Life-saving medication in critical situations

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Hydrocortisone Sodium Succinate For Injection BP is a sterile, clear solution of a corticosteroid with anti-inflammatory, immunosuppressive, and anti-allergic properties. It is widely used in emergency, ICU, and hospital settings to manage severe allergic reactions, shock, and inflammatory disorders. Manufactured according to British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and reliable pharmaceutical use.

Each 1 ml contains:

• Hydrocortisone Sodium Succinate BP – 100 mg / 200 mg (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Treatment of severe allergies and anaphylaxis

• Management of adrenal insufficiency and shock

• Anti-inflammatory therapy in autoimmune and inflammatory conditions

• Supportive therapy in critical care and sepsis

• Pre- and post-operative management of inflammatory conditions

• Administered intravenously (IV) or intramuscularly (IM)

• Dosage as prescribed by a qualified healthcare professional

• For hospital use only

• Rapid onset of action

• BP-grade sterile formulation

• Widely used in emergency, ICU, and hospital care

• Reliable anti-inflammatory and immunosuppressive effects

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Furosemide For Injection BP is a sterile, clear solution of a loop diuretic used to manage edema and fluid overload associated with heart failure, renal disease, and liver cirrhosis. It promotes rapid diuresis by inhibiting sodium and chloride reabsorption in the kidneys. Manufactured in compliance with British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and effective hospital use.

Each 1 ml contains:

• Furosemide BP – 10 mg / 20 mg (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Management of edema associated with heart, liver, or kidney disease

• Treatment of acute pulmonary edema

• Management of hypertension in emergency cases

• Supportive therapy in critical care fluid management

• Administered intravenously (IV) or intramuscularly (IM)

• Dosage as prescribed by a qualified healthcare professional

• For hospital and clinical use only

• Rapid onset of diuretic action

• BP-grade sterile formulation

• Widely used in ICU, emergency, and hospital care

• Effective management of fluid overload and edema

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Magnesium Sulphate For Injection BP is a sterile, clear solution used as an electrolyte replenisher and anticonvulsant in hospital and emergency settings. It plays a vital role in managing magnesium deficiency, eclampsia, pre-eclampsia, and cardiac arrhythmias. Manufactured according to British Pharmacopoeia (BP) standards, ensuring safe, high-quality, and effective pharmaceutical use.

Each 1 ml contains:

• Magnesium Sulphate BP – 50 mg / 100 mg (strength may vary)

• Water for Injection IP – q.s.

• Management of magnesium deficiency

• Prevention and treatment of eclampsia and pre-eclampsia

• Treatment of cardiac arrhythmias

• Supportive therapy in critical care and ICU

• Administered intravenously (IV) or intramuscularly (IM)

• Dosage as prescribed by a qualified healthcare professional

• For hospital and emergency use only

• Rapid replenishment of magnesium

• BP-grade sterile formulation

• Widely used in ICU, obstetrics, and emergency care

• Essential for electrolyte balance and seizure prevention

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Calcium Gluconate For Injection BP is a sterile, clear solution used as a calcium supplement and electrolyte replenisher in hospital and emergency settings. It is widely used to treat hypocalcemia, tetany, cardiac arrhythmias, and calcium deficiency. Manufactured according to British Pharmacopoeia (BP) standards, ensuring safe, high-quality, and reliable pharmaceutical use.

Each 1 ml contains:

• Calcium Gluconate BP – 100 mg / 500 mg (strength may vary)

• Water for Injection IP – q.s.

• Management of hypocalcemia and calcium deficiency

• Treatment of tetany and convulsions

• Supportive therapy in cardiac arrhythmias and electrolyte imbalance

• Emergency therapy in ICU and hospital care

• Administered intravenously (IV) slowly via controlled infusion

• Dosage as prescribed by a qualified healthcare professional

• For hospital and emergency use only

• Rapid replenishment of calcium

• BP-grade sterile formulation

• Widely used in ICU, emergency, and hospital care

• Essential for cardiac, neuromuscular, and skeletal health

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label

Phenytoin Sodium For Injection BP is a sterile, clear solution of a hydantoin-class antiepileptic drug used for the management and prevention of seizures in hospital and emergency settings. It works by stabilizing neuronal membranes and controlling abnormal electrical activity in the brain, making it effective in tonic-clonic and partial seizures. Manufactured according to British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and reliable use.

Each 1 ml contains:

• Phenytoin Sodium BP – 50 mg / 100 mg (strength may vary)

• Sodium Chloride IP, Water for Injection IP, Propylene Glycol IP – q.s.

• Management of tonic-clonic (grand mal) seizures

• Treatment of partial seizures

• Prevention and control of status epilepticus

• Emergency therapy in hospital and ICU settings

• Administered intravenously (IV) slowly via controlled infusion

• Dosage as prescribed by a qualified healthcare professional

• For hospital and emergency use only

• Rapid and effective seizure control

• BP-grade sterile formulation

• Suitable for acute and emergency seizure management

• Widely used in ICU, neurology, and hospital care

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label

Dobutamine For Injection BP is a sterile, clear solution of a synthetic catecholamine used in critical care and emergency settings. It acts as a positive inotropic agent, improving cardiac output and myocardial contractility in patients with heart failure, cardiogenic shock, or low cardiac output states. Manufactured according to British Pharmacopoeia (BP) standards, ensuring high-quality, safe, and reliable hospital use.

Each 1 ml contains:

• Dobutamine Hydrochloride BP – 12.5 mg / ml (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Management of acute heart failure

• Support in cardiogenic shock or low cardiac output states

• Emergency therapy in ICU and critical care

• Hemodynamic support during cardiac surgery

• Administered intravenously (IV) via controlled infusion

• Dosage and rate as prescribed by a qualified healthcare professional

• For hospital and critical care use only

• Rapid positive inotropic effect

• BP-grade sterile formulation

• Widely used in ICU, emergency, and hospital care

• Essential for life-saving cardiac support

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Mannitol For Injection BP is a sterile, clear solution of a osmotic diuretic used in emergency, ICU, and hospital settings. It helps to reduce intracranial and intraocular pressure and promotes diuresis in patients with acute kidney injury or fluid overload. Manufactured according to British Pharmacopoeia (BP) standards, ensuring safe, high-quality, and reliable pharmaceutical use.

Each 100 ml contains:

• Mannitol IP/BP – 10 g / 20 g / 25 g (strength may vary)

• Water for Injection IP – q.s.

• Reduction of intracranial pressure in cerebral edema

• Management of elevated intraocular pressure

• Promotion of diuresis in acute renal failure

• Supportive therapy in critical care and emergency medicine

• Administered intravenously (IV) via controlled infusion

• Dosage and rate as prescribed by a qualified healthcare professional

• For hospital and critical care use only

• Rapid osmotic diuretic effect

• BP-grade sterile formulation

• Widely used in ICU, emergency, neurology, and ophthalmology care

• Essential for management of intracranial and intraocular pressure

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in vials or infusion bottles

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label

Levetiracetam For Injection BP is a sterile, clear solution of a broad-spectrum antiepileptic drug (AED) used in hospital and emergency settings for the management of epileptic seizures. It works by modulating neurotransmitter release in the central nervous system, helping to control both partial-onset and generalized seizures. Manufactured according to British Pharmacopoeia (BP) standards, ensuring safe, high-quality, and effective use.

Each 1 ml contains:

• Levetiracetam BP – 100 mg / 500 mg (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Management of partial-onset seizures

• Treatment of generalized tonic-clonic seizures

• Adjunct therapy in hospital and emergency care for epilepsy

• Seizure control in acute neurological conditions

• Administered intravenously (IV) via controlled infusion

• Dosage as prescribed by a qualified healthcare professional

• For hospital and emergency use only

• Rapid onset of antiepileptic action

• BP-grade sterile formulation

• Suitable for acute seizure management in hospitals

• Widely used in ICU, neurology, and emergency care

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.

Noradrenaline For Injection BP is a sterile, clear solution of a catecholamine used in critical care and emergency settings. It acts as a potent vasopressor, helping to increase blood pressure and cardiac output in patients with shock, hypotension, or severe cardiovascular instability. Manufactured in compliance with British Pharmacopoeia (BP) standards, ensuring safe, high-quality, and reliable hospital use.

Each 1 ml contains:

• Noradrenaline (Norepinephrine) Tartrate BP – 1 mg / ml (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Management of acute hypotension and shock

• Support in septic, cardiogenic, or neurogenic shock

• Emergency therapy in ICU and critical care

• Maintenance of hemodynamic stability

• Administered intravenously (IV) via controlled infusion

• Dosage and rate as prescribed by a qualified healthcare professional

• For hospital and critical care use only

• Rapid and reliable vasopressor effect

• BP-grade sterile formulation

• Widely used in ICU, emergency, and hospital care

• Essential for life-saving cardiovascular support

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label

Dopamine For Injection BP is a sterile, clear solution of a catecholamine used in critical care and emergency settings. It acts as a cardiovascular and renal support agent, helping to increase cardiac output, improve blood pressure, and enhance renal perfusion in patients with shock, heart failure, or hypotension. Manufactured according to British Pharmacopoeia (BP) standards, ensuring safe, high-quality, and reliable hospital use.

Each 1 ml contains:

• Dopamine Hydrochloride BP – 40 mg / ml (strength may vary)

• Sodium Chloride IP, Water for Injection IP – q.s.

• Management of shock and hypotension

• Support in cardiogenic, septic, or neurogenic shock

• Enhancement of renal perfusion in acute kidney injury

• Emergency therapy in ICU and critical care

• Administered intravenously (IV) via controlled infusion

• Dosage and rate as prescribed by a qualified healthcare professional

• For hospital and critical care use only

• Rapid onset of cardiovascular support

• BP-grade sterile formulation

• Widely used in ICU, emergency, and hospital care

• Essential for life-saving hemodynamic management

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in ampoules or vials

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label

Iron Sucrose For Injection BP is a sterile, clear solution of an iron preparation used to treat iron deficiency anemia, especially in patients with chronic kidney disease or those intolerant to oral iron therapy. It provides a reliable source of elemental iron for red blood cell production and hemoglobin synthesis. Manufactured in compliance with British Pharmacopoeia (BP) standards, ensuring safe, high-quality, and effective hospital use.

Each 1 ml contains:

• Iron Sucrose BP – 20 mg / 100 mg (strength may vary)

• Water for Injection IP – q.s.

• Treatment of iron deficiency anemia

• Management of anemia in chronic kidney disease

• Supportive therapy for patients intolerant to oral iron therapy

• Correction of iron deficiency prior to surgery

• Administered intravenously (IV) via controlled infusion

• Dosage as prescribed by a qualified healthcare professional

• For hospital and clinical use only

• Rapid and effective iron replenishment

• BP-grade sterile formulation

• Widely used in ICU, nephrology, and hospital care

• Safe alternative to oral iron preparations

• Store in a cool, dry place, protected from light

• Keep out of reach of children

• Do not freeze

• Available in vials or ampoules

• Multiple pack sizes

• Tamper-evident, secure packaging

• 24–36 months, as per label.