FDA NDC Directory · JSON-LD · Markdown
NDC 37808-921 · HUMAN OTC DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | H E B |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA075010 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | IBUPROFEN (200 mg/1) |
| Marketing started | 19880524 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).