FDA NDC Directory · JSON-LD · Markdown

Danazol

NDC 71205-862 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077246
Dosage form / routeCAPSULE · ORAL
Active ingredientsDANAZOL (200 mg/1)
Marketing started20050928
Package count6

External sources

Source: openFDA. Public-domain (CC0).