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Ganirelix Acetate

NDC 71288-554 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214996
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsGANIRELIX ACETATE (250 ug/.5mL)
Marketing started20220606
Package count1

External sources

Source: openFDA. Public-domain (CC0).