FDA NDC Directory · JSON-LD · Markdown
NDC 0093-4136 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION
| Labeler / Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA065332 |
| Dosage form / route | POWDER, FOR SUSPENSION · ORAL |
| Active ingredients | CEFDINIR MONOHYDRATE (125 mg/5mL) |
| Marketing started | 20070508 |
| Package count | 2 |
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