Cefazolin 00143-9665
Product NDC
00143-9665- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 18, 2004
- Listing Expires
- December 31, 2026
- Application
- ANDA065143
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cefazolin Sodium | 20 g/1 |
Drug Class
Cephalosporin Antibacterial [EPC]Cephalosporins [CS]
Packaging Options(1)
1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9665-10)