FDA NDC Directory · JSON-LD · Markdown
NDC 71335-2145 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | Labetalol Hydrochloride |
|---|---|
| Labeler / Manufacturer | Bryant Ranch Prepack |
| Marketing category | Abbreviated NDA (generic) · App ANDA200908 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | LABETALOL HYDROCHLORIDE (100 mg/1) |
| Marketing started | 20120724 |
| Package count | 5 |
Source: openFDA. Public-domain (CC0).