Oxytetracycline Injection Grade
1. Core Quality & Specifications Complies with USP/EP/BP/CP international pharmacopoeia standards. As a sterile crystalline powder (yellow to yellowish-brown), key specs: Oxytetracycline content ≥95.0% (dried basis), sterility (no viable microbes), total impurities ≤5.0%, heavy metals ≤10 ppm, particle size customizable (typical D90 ≤100 μm). No additives, pure API for injection-grade use.
2. Antibacterial Efficacy Broad-spectrum bacteriostatic activity against gram-positive/negative bacteria (Staphylococcus aureus, E. coli, Vibrio spp.), mycoplasmas, rickettsiae. Acts by inhibiting bacterial protein synthesis. Retains full efficacy in final injectable formulations, enabling rapid absorption and long-lasting infection control in animals.
3. Applications & Formulation Specialized raw material for veterinary injectable products (solutions, lyophilized powders). Final formulations treat bacterial/mycoplasmal infections in livestock, poultry, and aquatic animals. Compatible with common injection excipients (propylene glycol, water for injection); use immediately after opening.
4. Packaging & Storage Sterile tamper-evident packaging: 1g-1kg glass vials/aluminum foil bags, 5-25kg cardboard drums. Store at 2-8°C (cool, dry, light-protected), shelf life 24 months sealed. Do not freeze; discard unused product within 24h of opening.
5. Core Advantages High purity & batch consistency; sterile grade (no extra sterilization needed); excellent stability; easy to formulate; broad antibacterial spectrum. Produced under GMP, with batch-specific COA available.
Key Note: For pharmaceutical manufacturing only; not for direct administration. Avoid mixing with penicillins/alkaline substances. GMP-compliant production, customizable specs and bulk orders available via sales team.
