FDA NDC Directory · JSON-LD · Markdown
NDC 72789-003 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE
| Labeler / Manufacturer | PD-Rx Pharmaceuticals, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA091432 |
| Dosage form / route | TABLET, DELAYED RELEASE · ORAL |
| Active ingredients | NAPROXEN (500 mg/1) |
| Marketing started | 20160705 |
| Package count | 1 |
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