Shivsrushti Surgimed Private Limited

Brand: XAVITAZ 2.5 MG Vial
Content / Active Ingredient: Ceftazidime 2 g + Avibactam 0.5 g (Powder for Concentrate for Solution for Injection)
Company / Manufacturer: BDR Pharmaceuticals International Pvt. Ltd.
Pack Size: 2.5 g Vial (Lyophilized Powder for Injection)

XAVITAZ 2.5 MG Injection is a sterile injectable antibiotic combination containing Ceftazidime 2 g and Avibactam 0.5 g. It is supplied as a lyophilized powder for reconstitution to prepare a solution for intravenous injection.

Ceftazidime is a third-generation cephalosporin antibiotic that inhibits bacterial cell wall synthesis, while Avibactam is a beta-lactamase inhibitor that protects Ceftazidime from degradation by resistant bacteria. This combination is particularly effective against multidrug-resistant Gram-negative bacterial infections and is commonly used in hospital and critical care settings.

·         Composition: Ceftazidime 2 g + Avibactam 0.5 g per vial

·         Therapeutic Category: Antibiotic – Cephalosporin & Beta-lactamase inhibitor combination

·         Dosage Form: Lyophilized powder for IV solution

·         Route of Administration: Intravenous (IV) use only

·         Prescription Status: Schedule H – Prescription medicine

·         Packaging: Single vial pack

·         Storage: Store in a cool, dry place below 30°C; protect from light

XAVITAZ 2.5 MG Injection is indicated for:

·         Complicated intra-abdominal infections

·         Complicated urinary tract infections, including pyelonephritis

·         Hospital-acquired pneumonia and ventilator-associated pneumonia

·         Severe infections caused by multidrug-resistant Gram-negative bacteria

Dosage and duration of therapy should be determined by a qualified healthcare professional based on infection severity and patient condition.

Ceftazidime inhibits bacterial cell wall synthesis, causing bacterial death. Avibactam protects Ceftazidime from enzymatic degradation by beta-lactamases, restoring its efficacy against resistant strains.

·         Administer only under medical supervision.

·         Monitor renal function during therapy.

·         Possible side effects include nausea, diarrhea, headache, rash, and injection-site reactions.

Use cautiously in patients with known beta-lactam allergy

BRAND NAME : FORTACEF 1 GM
CONTENT : CEFTAZIDIME 1 GM
COMPANY : TROIKAA PHARMACEUTICALS LTD

NITROPLUS 25 mg Injection by Neon Laboratories Ltd

·         Nitroglycerin Injection USP (also called Glyceryl Trinitrate) — 25 mg per 5 mL ampoule (which is 5 mg/mL of nitroglycerin).

Neon Laboratories Ltd — an Indian pharmaceutical company that manufactures injectable cardiovascular drugs.

·         Pack: 5 × 5 mL ampoules (i.e., five 5 mL sterile injectable ampoules per pack).

·         Prescription: Required — this is a hospital/clinical injectable medicine given by a clinician under supervision.

Nitroplus 25 mg Injection is a vasodilator that works by relaxing and widening blood vessels, increasing blood flow and reducing the workload on the heart. Its typical uses include:

·         Treatment and prevention of angina pectoris (chest pain due to reduced blood flow to the heart).

·         Management of acute hypertension or high blood pressure in surgical or emergency settings.

·         Support in conditions such as heart failure and myocardial infarction by improving circulation.

This medicine is administered intravenously under medical supervision.

Nitroglycerin (glyceryl trinitrate) is an organic nitrate that causes vasodilation (relaxation of blood vessels), which helps lower blood pressure and improves blood flow to the heart muscle. This can relieve chest pain and reduce the strain on the heart.

·         Must be administered by a healthcare professional (often by infusion into a vein).

·         Headache (very common)

·         Low blood pressure (hypotension)

·         Dizziness or light‑headedness

·         Flushing
These arise due to the vessel‑relaxing effect of nitroglycerin.

·         Avoid use with erectile dysfunction medicines (e.g., sildenafil) — may cause dangerously low blood pressure.

·         Use with caution in pregnancy and breastfeeding after consulting a doctor.

·         Class: Organic nitrate vasodilators

·         Therapeutic Use: Anti‑anginal / cardiovascular support

Brand Name: VPRESS 1 ML AMP
Content: Vasopressin Injection I.P. (antidiuretic hormone, parenteral formulation)
Company / Manufacturer: Neon Lab Ltd / Neon Laboratories Ltd (Indian pharmaceutical manufacturer)
Pack: 1 ml ampoule (typically containing 20 IU of vasopressin per ml)

VPRESS 1 ML Ampoule is a prescription medicine containing vasopressin, a naturally occurring antidiuretic hormone supplied as a sterile injectable solution for intravenous use. It is used in hospital and clinical settings under strict medical supervision.

·         Active Ingredient: Vasopressin (commonly available as 20 IU per 1 ml ampoule).

·         Form: Sterile injectable ampoule.

·         Administration: Administered by a healthcare professional via injection/infusion as directed by a doctor.

·         Prescription: Required (this is a hospital‑use cardiovascular/critical care medication).

VPRESS (Vasopressin Injection) is used for:

·         Management of diabetes insipidus — a condition of excessive urination due to lack of antidiuretic hormone.

·         Control of bleeding from esophageal varices — especially in patients with liver disease.

·         Support in hypotensive states / vasodilatory shock — to help raise blood pressure when fluids and other vasopressors are insufficient.

It works by binding to vasopressin receptors, promoting vasoconstriction (narrowing of blood vessels) and reducing urine output by increasing water reabsorption in the kidneys.

·         Clinical Use Only: Administered by qualified medical professionals in a hospital/critical care environment.

·         Possible Side Effects: May include headache, nausea, heart rate changes, low sodium levels (hyponatremia), injection site reactions, or circulatory issues — monitor under supervision.

·         Storage: Store as per label/medical guidance (often refrigerated between 2–8 °C and protected from light).

·         Not for Self‑Administration: This is not suitable for home use without clinical oversight.

📌 Category :- Cardiovascular / Critical Care Injectable – Vasopressor / Antidiuretic Hormone Therapy

📦 Product Overview

💊 Active Content

Sterile Noradrenaline Concentrate I.P.
Each 2 mL ampoule contains Noradrenaline (also called norepinephrine) 2 mg (i.e., 1 mg/mL).
Pack: 5 ampoules × 2 mL each

Manufacturer / Company: Neon Laboratories Ltd (NEON), India

🩺 What It Is
Norad Injection contains noradrenaline, a potent vasopressor and adrenergic agent used in emergency clinical settings. It is a prescription‑only injectable medicine administered under close medical supervision (usually in a hospital ICU or emergency room).

📋 Typical Uses
Noradrenaline works by narrowing (constricting) blood vessels, which increases blood pressure and improves blood flow to vital organs. It is commonly used for:

• Severe hypotension (low blood pressure) — especially in critical care
• Septic shock (life‑threatening infection causing dangerously low BP)
• Cardiogenic shock or cardiac arrest support
• During major surgery to maintain stable blood pressure
• Other shock states where blood pressure needs rapid stabilization

This injection is not for self‑administration, and must be given by a trained medical professional.

⚙️ How It Works
Noradrenaline stimulates alpha‑adrenergic receptors on blood vessel walls, causing them to tighten (vasoconstriction). This increases systemic vascular resistance and raises blood pressure. It also supports the heart’s pumping action to help maintain circulation.

⚠️ Safety and Side Effects
Important precautions:

Used only in hospital or emergency medical settings under close monitoring.
Must be administered intravenously (into a vein).
Monitor heart rate, blood pressure and organ perfusion during use.

Possible side effects may include:

• High blood pressure or rapid heart rate
• Headache, anxiety, tremors
• Tissue damage if the drug leaks outside the vein (extravasation)

ARTACIL 50mg/5ml Injection – Atracurium Besylate Injection I.P.

Brand Name: ARTACIL 50mg/5ml
Generic Name: Atracurium Besylate Injection I.P.
Strength: 50 mg / 5 ml
Dosage Form: Injection
Manufacturer: Neon Laboratories Limited
Packaging: Standard company packing

ARTACIL 50mg/5ml Injection contains Atracurium Besylate, a non-depolarizing neuromuscular blocking agent used as an adjunct to general anesthesia. It is indicated for facilitating endotracheal intubation and providing skeletal muscle relaxation during surgical procedures or controlled ventilation.

Atracurium Besylate ensures effective and predictable neuromuscular blockade when administered under proper medical supervision in hospital settings.

·         Endotracheal intubation

·         Muscle relaxation during surgeries

·         ICU sedation and ventilation support

·         Adjunct to general anesthesia

·         Intermediate duration of action

·         Reliable neuromuscular blockade

·         Suitable for hospital and institutional supply

·         Manufactured under stringent GMP standards

Note: For use by qualified anesthesiologists or trained healthcare professionals only.

Brand: BIAPEN 300 MG Vial
Content / Active Ingredient: Biapenem for Injection 300 mg
Company / Manufacturer: BDR Pharmaceutical Ltd
Pack Size: 300 mg Vial (Lyophilized Powder for Injection)

BIAPEN 300 MG Injection is a sterile injectable formulation containing Biapenem 300 mg, a broad-spectrum carbapenem-class antibiotic used for the treatment of serious bacterial infections. It is supplied as a lyophilized powder for reconstitution and intended for intravenous administration under medical supervision.

Biapenem is effective against a wide range of Gram-positive and Gram-negative bacteria, including many multidrug-resistant strains, making it suitable for hospital and critical care settings.

·         Composition: Biapenem 300 mg per vial

·         Therapeutic Category: Antibiotic – Carbapenem class

·         Dosage Form: Sterile lyophilized powder for IV injection/infusion

·         Route of Administration: Intravenous (IV) use only

·         Prescription Status: Schedule H – Prescription medicine

·         Packaging: Single vial pack

·         Storage: Store in a cool, dry place below recommended temperature

BIAPEN 300 MG Injection is indicated for the treatment of:

·         Respiratory tract infections

·         Urinary tract infections

·         Intra-abdominal infections

·         Skin and soft tissue infections

·         Septicemia (bloodstream infections)

·         Hospital-acquired infections

Dosage and duration should be determined by a qualified healthcare professional based on infection severity and patient condition.

Biapenem inhibits bacterial cell wall synthesis, leading to bacterial cell death. Its broad-spectrum activity makes it effective against both Gram-positive and Gram-negative organisms, including resistant strains.

·         To be administered only under strict medical supervision.

·         Monitor renal function during therapy.

·         Possible side effects include nausea, diarrhea, headache, rash, and injection-site reactions.

Brand: I-MAN 500
Content / Active Ingredient: Imipenem & Cilastatin for Injection IP
Strength: 500 mg (Imipenem 500 mg + Cilastatin 500 mg as per standard formulation)
Company / Manufacturer: BDR Pharmaceuticals
Pack Size: 1 Vial (Dry Powder for Injection)

I-MAN 500 Injection is a sterile, broad-spectrum carbapenem antibiotic combination containing Imipenem and Cilastatin. It is supplied as a dry powder for reconstitution and intended for intravenous administration under medical supervision.

Imipenem is a powerful beta-lactam antibiotic effective against a wide range of Gram-positive and Gram-negative bacteria. Cilastatin is a renal dehydropeptidase inhibitor that prevents the breakdown of Imipenem in the kidneys, thereby enhancing its effectiveness and duration of action.

This formulation is widely used in hospital settings for the treatment of severe and life-threatening bacterial infections.

·         Composition: Imipenem & Cilastatin for Injection IP

·         Strength: 500 mg per vial

·         Therapeutic Category: Antibiotic – Carbapenem class

·         Dosage Form: Sterile dry powder for IV infusion

·         Route of Administration: Intravenous (IV) use only

·         Prescription Status: Schedule H – Prescription medicine

·         Packaging: 1 Vial pack

·         Storage: Store in a cool, dry place below recommended temperature

I-MAN 500 Injection is indicated for the treatment of:

·         Severe respiratory tract infections

·         Complicated urinary tract infections

·         Intra-abdominal infections

·         Septicemia (bloodstream infections)

·         Skin and soft tissue infections

·         Gynecological infections

Dosage and duration should be determined by a qualified healthcare professional based on infection severity and patient condition.

Imipenem inhibits bacterial cell wall synthesis leading to bacterial death. Cilastatin protects Imipenem from enzymatic degradation in the kidneys, ensuring optimal therapeutic levels in the body.

For Bulk Quantity Rates Will Be Negotiable

Content: Amiodarone Sterile Concentrate I.P.
Company: Neon
Pack: 5×5 ampoules of 3 ml

Amiodon Injection 3 ml (similar injectable amiodarone product used in India) is a sterile injectable formulation of Amiodarone Hydrochloride, an anti-arrhythmic medicine used to treat serious irregular heart rhythms (arrhythmias) in hospital settings.

·         Amiodarone Hydrochloride I.P. – 150 mg in each 3 ml ampoule (50 mg/ml).
This is the same active component described in “Amiodone 150/3 ml”.

·         Anti-arrhythmic (Cardiac medicine) – used to manage life-threatening cardiac arrhythmias such as:

o    Atrial fibrillation / flutter

o    Ventricular tachycardia

o    Other fast or uneven heartbeats when rapid control is required or oral drugs can’t be used.

Amiodarone works by blocking abnormal electrical signals in the heart that cause irregular heart rhythms, helping to stabilize the heartbeat.

·         Intravenous (IV) via injection or infusion by a doctor or trained nurse in a hospital or emergency setting.

·         Dosage and rate are determined by the physician based on the patient’s condition.

·         Should only be given in a hospital under continuous monitoring (ECG, blood pressure, etc.).

·         Not recommended in patients with allergy to amiodarone or iodine, certain heart blocks, severe breathing issues, or without appropriate medical supervision.

·         Use with caution in people with liver, lung, or thyroid problems.

Some effects that may occur (especially with IV use) include:

·         Low blood pressure, slow heartbeat

·         Blurred vision or halos

·         Irritation at injection site

·         Skin photosensitivity (sensitivity to sunlight)
Most side effects depend on dose and clinical situation.

Stored as directed on the label; typically kept protected from light and below 25 °C.

BRAND NAME : DOPACIN 5ML
CONTENT : DOPAMINE HYDROCHLORIDE 40MG

COMPANY : TROIKAA PHARMACEUTICALS LTD