Cefazolin Sodium is a high-potency sodium salt form of Cefazolin, a premier β-lactam antibiotic within the cephalosporin class. Engineered for exceptional antibacterial efficacy, it is specifically optimized to combat staphylococci and streptococci, serving as a critical pharmaceutical component for preoperative prophylaxis and the treatment of moderate bacterial infections.
Renowned for its rapid therapeutic onset and an impressive safety profile, Cefazolin Sodium is a cornerstone in surgical and emergency medicine. Its stability in solution and reliable spectrum of activity make it the ideal active pharmaceutical ingredient (API) for sterile injectable formulations targeting the skin, bone, urinary tract, and respiratory system.
Detailed Parameters
| Chemical Name | Cefazolin Sodium | CAS Number | 27164-46-1 |
|---|---|---|---|
| Pharmacological Class | Cephalosporin (β-lactam) | Primary Target | Staphylococci & Streptococci |
| Application Type | Pharmaceutical API | Dosage Form | Sterile Injectable |
| Packaging Type | Fiber Drums/Glass Vials | Standard Size | 10 kg to 25 kg per drum |
| Storage Condition | Cool, dry, ventilated area | Sensitivity | Moisture and Light Sensitive |
Key Advantages
Broad Spectrum Activity
Exceptional effectiveness against a wide range of Gram-positive bacteria, ensuring reliable clinical outcomes.
Rapid Therapeutic Action
Engineered for fast-acting delivery, making it essential for urgent preoperative prophylaxis.
High Purity Grade
Manufactured to strict pharmaceutical standards to ensure minimal impurities and maximum safety.
Excellent Stability
Superior stability in reconstituted solution, maintaining potency during clinical administration.
Proven Safety Profile
Well-documented tolerance and safety, reducing risks in acute care and surgical settings.
Flexible Packaging
Available in pharmaceutical-grade fiber drums or customized sterile vials to fit your production line.
Product Gallery
Management Platforms
Quality Assurance
Rigorous batch testing following international pharmacopeial standards for absolute purity.
Sterile Production
Processed in clean-room environments to prevent contamination in injectable-grade APIs.
Supply Chain Stability
Optimized logistics ensuring consistent availability of raw materials for pharma manufacturers.
Regulatory Compliance
Complete documentation support including COA and MSDS for seamless customs clearance.
Storage Control
Climate-controlled warehousing to preserve the chemical potency of sensitive antibiotics.
Custom Synthesis
Ability to adjust packaging and specifications based on specific manufacturing requirements.
Investment Return Comparison
| Performance Metric | Standard Grade API | Premium Cefazolin Sodium |
|---|---|---|
| Purity Level | Standard Pharma Grade | Ultra-High Purity |
| Reaction Speed | Moderate | Fast-Acting Effect |
| Stability Period | Baseline | Extended Shelf-life |
| Contamination Risk | Low | Ultra-Low (Sterile) |
| Clinical Efficacy | Conventional | Enhanced Bioavailability |
Frequently Asked Questions
It is primarily used as an active ingredient in sterile injectable formulations for perioperative prophylaxis and treating infections of the skin, bone, urinary tract, and respiratory system.
The product should be stored in a cool, dry, and well-ventilated area, strictly kept away from moisture and direct light to preserve its potency.
Standard bulk packaging consists of double polyethylene bags inside fiber drums, typically ranging from 10 kg to 25 kg per drum.
Yes, we provide customized packaging options, including sterile glass vials, to meet the specific requirements of pharmaceutical manufacturing lines.
It exhibits excellent antibacterial activity particularly against staphylococci and streptococci species.
It is typically reconstituted using sterile water for injection or other suitable solvents, following strict pharmacopeial guidelines and sterile conditions.
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