FDA NDC Directory · JSON-LD · Markdown
NDC 29300-252 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Unichem Pharmaceuticals (USA), Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA212719 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | LABETALOL HYDROCHLORIDE (100 mg/1) |
| Marketing started | 20221001 |
| Package count | 2 |
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