FDA NDC Directory · JSON-LD · Markdown

Carvedilol

NDC 70518-4389 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA077614
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCARVEDILOL (12.5 mg/1)
Marketing started20250708
Package count2

External sources

Source: openFDA. Public-domain (CC0).