FDA NDC Directory · JSON-LD · Markdown
NDC 69306-266 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Doc Rx |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA211890 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | FAMOTIDINE (26.6 mg/1) IBUPROFEN (800 mg/1) |
| Marketing started | 20210804 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).