FDA NDC Directory · JSON-LD · Markdown

Carvedilol

NDC 0904-7307 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA078251
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCARVEDILOL (12.5 mg/1)
Marketing started20240913
Package count1

External sources

Source: openFDA. Public-domain (CC0).