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Vancomycin Hydrochloride for Injection USP 500mg is a sterile powder specifically formulated for intravenous administration, designed to combat severe bacterial infections caused by Gram-positive pathogens. Manufactured adhering strictly to the United States Pharmacopeia (USP) standards, this glycopeptide antibiotic offers potent efficacy against resistant strains such as MRSA. The 500mg dosage strength ensures versatility in clinical dosing regimens across hospitals and healthcare facilities. Packaged in a single vial, this powder for injection guarantees ease of use and maintains sterility until reconstitution, making it ideal for hospital pharmacies and healthcare suppliers requiring reliable and quality-assured antibiotic formulations.
Key Features
| Features | Description |
|---|---|
| Strength | 500mg |
| Dosage Form | Powder for Injection |
| Pharmacopeia Standard | United States Pharmacopeia (USP) |
| Therapeutic Category | Glycopeptide Antibiotics |
| Pack Type | Vial |
| Pack Details | Single Unit Pack |
| Sterility | Sterile Powder |
| Intended Use | Intravenous Injection |
| Manufacturer | Ancalima Lifesciences Limited |
| MOQ | 1 vial |
| Attributes | Description |
|---|---|
| Active Ingredient | Vancomycin Hydrochloride |
| Dosage Strength | 500mg per vial |
| Formulation | Sterile powder for reconstitution |
| Compliance | Meets USP standards |
| Therapeutic Class | Glycopeptide antibiotic |
| Packaging | Single vial per pack |
| Intended Route | Intravenous injection |
| Storage Conditions | Store in a cool, dry place, protected from light |
| Shelf Life | Refer to label/packaging |
| Manufacturer | Ancalima Lifesciences Limited |
*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, each pack contains a single unit vial of 500mg Vancomycin Hydrochloride sterile powder for injection.
Yes, this product meets all United States Pharmacopeia (USP) requirements ensuring high-quality and purity.
Yes, Vancomycin Hydrochloride powder is intended for intravenous injection after proper reconstitution as per guidelines.
The minimum order quantity for Vancomycin Hydrochloride for Injection USP 500mg is 1 vial.
Yes, as a glycopeptide antibiotic, Vancomycin Hydrochloride is often prescribed for serious infections caused by MRSA and other resistant Gram-positive bacteria.
Country Of Origin: India
Vancomycin Hydrochloride Injection USP is a biocompatible parenteral antibiotic formulation, delivering precise 500mg dosage per vial for systemic bacterial infection management.
The standardized 500mg volume allows repeatable dosing and predictable therapeutic performance in clinical applications.
Vancomycin Hydrochloride Injection USP contains pharmaceutically pure Vancomycin hydrochloride in sterile isotonic aqueous medium. Stabilizers prevent degradation and maintain solubility, ensuring uniform parenteral administration and reliable dosage delivery.
The injectable exhibits predictable pharmacokinetics and low-viscosity flow suitable for intravenous or intramuscular delivery. Stability under ambient and refrigerated conditions ensures consistent clinical performance across institutional and bulk use.
Widely used in hospitals, clinics, and institutional procurement, Vancomycin Hydrochloride Injection USP supports bulk and OEM supply, export markets, and regulated pharmaceutical channels. Its standardized 500mg dosage ensures reproducible therapeutic outcomes for professional medical applications.
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