FDA NDC Directory · JSON-LD · Markdown
NDC 51655-275 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Northwind Health Company, LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA090796 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | IBUPROFEN (800 mg/1) |
| Marketing started | 20200616 |
| Package count | 5 |
Source: openFDA. Public-domain (CC0).