FDA NDC Directory · JSON-LD · Markdown

Carvedilol

NDC 65862-142 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078332
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCARVEDILOL (3.125 mg/1)
Marketing started20070905
Package count3

External sources

Source: openFDA. Public-domain (CC0).