FDA NDC Directory · JSON-LD · Markdown
NDC 51655-202 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Northwind Health Company, LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA078212 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | BENAZEPRIL HYDROCHLORIDE (10 mg/1) |
| Marketing started | 20230315 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).