FDA NDC Directory · JSON-LD · Markdown
NDC 50090-7763 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE
| Labeler / Manufacturer | A-S Medication Solutions |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA078853 |
| Dosage form / route | TABLET, DELAYED RELEASE · ORAL |
| Active ingredients | DIVALPROEX SODIUM (250 mg/1) |
| Marketing started | 20240626 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).