FDA NDC Directory · JSON-LD · Markdown

AMBRISENTAN

NDC 42794-052 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSigmapharm Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208354
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMBRISENTAN (10 mg/1)
Marketing started20190410
Package count2

External sources

Source: openFDA. Public-domain (CC0).