FDA NDC Directory · JSON-LD · Markdown

Ambrisentan

NDC 70710-1180 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210058
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMBRISENTAN (10 mg/1)
Marketing started20190412
Package count5

External sources

Source: openFDA. Public-domain (CC0).