Cefoxitin 00143-9878
Product NDC
00143-9878- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- March 12, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA065238
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cefoxitin Sodium | 1 g/1 |
Drug Class
Cephalosporin Antibacterial [EPC]Cephalosporins [CS]
Packaging Options(1)
25 VIAL in 1 CARTON (0143-9878-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9878-01)