Cefazolin 00781-3450
Product NDC
00781-3450- Manufacturer
- Sandoz Inc
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intramuscular, Intravenous, And Parenteral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 9, 1988
- Listing Expires
- December 31, 2027
- Application
- ANDA062831
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cefazolin Sodium | 500 mg/1 |
Drug Class
Cephalosporin Antibacterial [EPC]Cephalosporins [CS]