FDA NDC Directory · JSON-LD · Markdown

Carvedilol

NDC 43063-833 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078332
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCARVEDILOL (6.25 mg/1)
Marketing started20070905
Package count1

External sources

Source: openFDA. Public-domain (CC0).