FDA NDC Directory · JSON-LD · Markdown

EXEMESTANE

NDC 70301-2017 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerOPKO Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA200898
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsEXEMESTANE (25 mg/1)
Marketing started20260930
Package count1

External sources

Source: openFDA. Public-domain (CC0).