FDA NDC Directory · JSON-LD · Markdown
NDC 55111-533 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE
| Labeler / Manufacturer | Dr. Reddy's Laboratories Ltd |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA090161 |
| Dosage form / route | TABLET, EXTENDED RELEASE · ORAL |
| Active ingredients | DIVALPROEX SODIUM (250 mg/1) |
| Marketing started | 20130811 |
| Package count | 5 |
Source: openFDA. Public-domain (CC0).