FDA NDC Directory · JSON-LD · Markdown

Anastrozole

NDC 68382-209 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078921
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsANASTROZOLE (1 mg/1)
Marketing started20100627
Package count2

External sources

Source: openFDA. Public-domain (CC0).