MEFOXIN (CEFOXITIN SODIUM) — FDA Approval NDA050517 (PHARMOBEDIENT)
MEFOXIN (CEFOXITIN SODIUM) — FDA Approval NDA050517 (PHARMOBEDIENT) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: MEFOXIN; Active ingredients: CEFOXITIN SODIUM; Application number: NDA050517.
| Brand name | MEFOXIN |
|---|---|
| Active ingredients | CEFOXITIN SODIUM |
| Application number | NDA050517 |
| Sponsor | PHARMOBEDIENT |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Marketing status | Discontinued |
| Products in application | 3 |
| First approval date | 19781018 |
| Source | openFDA Drugs@FDA |
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