FDA NDC Directory · JSON-LD · Markdown

Anastrozole

NDC 72789-342 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078921
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsANASTROZOLE (1 mg/1)
Marketing started20100627
Package count1

External sources

Source: openFDA. Public-domain (CC0).