FDA NDC Directory · JSON-LD · Markdown

LEUPROLIDE ACETATE

NDC 42023-259 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217437
Dosage form / routeINJECTION · SUBCUTANEOUS
Active ingredientsLEUPROLIDE ACETATE (1 mg/.2mL)
Marketing started20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).