FDA NDC Directory · JSON-LD · Markdown

CARVEDILOL

NDC 68788-8231 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078165
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCARVEDILOL (25 mg/1)
Marketing started20220808
Package count3

External sources

Source: openFDA. Public-domain (CC0).