FDA NDC Directory · JSON-LD · Markdown

Carvedilol

NDC 68788-8252 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077614
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCARVEDILOL (3.125 mg/1)
Marketing started20220902
Package count5

External sources

Source: openFDA. Public-domain (CC0).