FDA NDC Directory · JSON-LD · Markdown
NDC 70954-784 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | ANI Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA219118 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | NABUMETONE (500 mg/1) |
| Marketing started | 20250107 |
| Package count | 2 |
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