FDA NDC Directory · JSON-LD · Markdown
NDC 30698-453 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | benazepril hydrochloride and hydrochlorothiazide |
|---|---|
| Labeler / Manufacturer | Validus Pharmaceuticals LLC |
| Marketing category | New Drug Application (innovator) · App NDA020033 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | BENAZEPRIL HYDROCHLORIDE (20 mg/1) HYDROCHLOROTHIAZIDE (12.5 mg/1) |
| Marketing started | 19920530 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).