FDA NDC Directory · JSON-LD · Markdown
NDC 55111-529 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE
| Labeler / Manufacturer | Dr.Reddy's Laboratories Limited |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA078755 |
| Dosage form / route | TABLET, DELAYED RELEASE · ORAL |
| Active ingredients | DIVALPROEX SODIUM (125 mg/1) |
| Marketing started | 20080729 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).