FDA NDC Directory · JSON-LD · Markdown
NDC 37835-585 · HUMAN OTC DRUG · TABLET
| Labeler / Manufacturer | BI-MART |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA079174 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | IBUPROFEN (200 mg/1) |
| Marketing started | 20250201 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).