FDA NDC Directory · JSON-LD · Markdown

Labetalol Hydrochloride

NDC 60687-461 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA207743
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLABETALOL HYDROCHLORIDE (300 mg/1)
Marketing started20190716
Package count1

External sources

Source: openFDA. Public-domain (CC0).