FDA NDC Directory · JSON-LD · Markdown
NDC 0093-0109 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA070541 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | CARBAMAZEPINE (200 mg/1) |
| Marketing started | 19900930 |
| Marketing ended | 20260731 |
| Package count | 2 |
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