FDA NDC Directory · JSON-LD · Markdown
NDC 72603-260 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Labeler / Manufacturer | NorthStar Rx LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA078979 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | DIVALPROEX SODIUM (125 mg/1) |
| Marketing started | 20240801 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).