Cefoxitin 25021-0110
Product NDC
25021-0110- Manufacturer
- Sagent Pharmaceuticals
- Dosage Form
- Injection, Powder, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- November 5, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA065414
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cefoxitin Sodium | 2 g/1 |
Drug Class
Cephalosporin Antibacterial [EPC]Cephalosporins [CS]
Packaging Options(1)
10 VIAL in 1 CARTON (25021-110-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL