Vancomycin Hydrochloride for Injection USP 500mg
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Country Of Origin : India
Vancomycin Hydrochloride for Injection USP
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.
Key Features:
- Optimized injectable for rapid systemic absorption
- 500mg active concentration per vial
- Maintains chemical and physical stability under storage
- Minimized injection discomfort with controlled osmolarity
Attributes:
- 500mg dosage for reproducible therapeutic efficacy
- Injectable formulation with controlled solubility
- Regulatory-compliant for hospital and institutional use
Composition and Formulation Details
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.
Functional Characteristics and Performance
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.
Application and Industry Relevance
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.
