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Vancomycin Hydrochloride for Injection USP 1gm is a sterile, lyophilized powder formulated specifically for intravenous administration to treat serious gram-positive bacterial infections. Each vial contains 1 gram of Vancomycin Hydrochloride, adhering to the United States Pharmacopeia (USP) standards, ensuring high purity and efficacy. This potent glycopeptide antibiotic is widely used in clinical settings for managing infections caused by methicillin-resistant Staphylococcus aureus (MRSA) and other resistant gram-positive pathogens. The product's single-unit vial packaging guarantees ease of use, safety, and precise dosing in hospital pharmacies and healthcare institutions. Being a sterile injection powder, it requires reconstitution with an appropriate diluent before administration, facilitating rapid and effective systemic delivery for critically ill patients. Vancomycin Hydrochloride for Injection USP 1gm is indispensable in therapeutic protocols where resistant bacterial infections pose significant health risks, making it a vital asset for healthcare providers focusing on critical infection control.
Key Features
| Features | Description |
|---|---|
| Active Ingredient | Vancomycin Hydrochloride |
| Strength | 1 gram per vial |
| Dosage Form | Sterile Powder for Injection |
| Pharmacopeia Compliance | United States Pharmacopeia (USP) Standard |
| Therapeutic Category | Glycopeptide Antibiotics |
| Pack Type | Single Unit Vial |
| Indications | Treatment of serious gram-positive bacterial infections including MRSA |
| Administration Route | Intravenous after reconstitution |
| Packaging Details | Single vial pack for precise dosing |
| Sterility | Sterile and ready for reconstitution |
| Attributes | Description |
|---|---|
| Vancomycin Content | 1gm per vial |
| Form | Lyophilized Powder |
| Compliance | USP certified product |
| Packaging | Single-use vial |
| Storage Conditions | Store below 30°C; protected from moisture |
| Reconstitution | Requires reconstitution with prescribed diluent |
| Shelf Life | Typically 2 years from manufacturing date |
| Therapeutic Use | Used against MRSA and other resistant gram-positive infections |
*Disclaimer: The above description has been AI-generated and has not been audited or verified for accuracy. It is recommended to verify product details independently before making any purchasing decisions.
Yes, Vancomycin Hydrochloride for Injection USP 1gm is typically compatible with standard sterile water for injection and 0.9% sodium chloride solution for reconstitution before intravenous administration.
The product should be stored below 30°C in a dry place, protected from moisture and light to maintain its stability and efficacy.
No, it requires reconstitution with an appropriate sterile diluent prior to intravenous injection.
Yes, it is effective against a broad range of serious gram-positive bacterial infections resistant to other antibiotics.
Hospitals, clinics, and healthcare institutions managing severe bacterial infections including ICUs and infectious disease centers frequently require Vancomycin Hydrochloride for Injection USP 1gm due to its efficacy against resistant pathogens.
Country Of Origin: India
Vancomycin Hydrochloride Injection USP is a biocompatible parenteral antibiotic formulation designed for systemic bacterial infection management, delivering a precise 1gm dosage per vial for clinical reliability.
The standardized 1gm unit volume allows consistent therapeutic delivery, ensuring predictable pharmacodynamic outcomes in hospital and institutional applications.
Vancomycin Hydrochloride Injection USP 1gm contains pharmaceutically pure Vancomycin hydrochloride dissolved in sterile isotonic aqueous media. Stabilizers maintain solubility, prevent degradation, and support homogeneity, ensuring precise dosing for intravenous or intramuscular administration.
The formulation provides consistent pharmacokinetics, predictable bioavailability, and low-viscosity flow for smooth administration. Stability under both ambient and refrigerated conditions ensures reliable performance across bulk, institutional, and export-use scenarios.
Widely employed in hospital pharmacies, clinical environments, and institutional procurement channels, this 1gm vial is ideal for bulk sourcing, OEM supply, and export-ready pharmaceutical operations. Its standardized dosage and professional-grade formulation support regulated B2B markets, ensuring consistent systemic antibacterial therapy.
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