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Fulvestrant

NDC 43598-262 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerDr.Reddy's Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA209246
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR
Active ingredientsFULVESTRANT (50 mg/mL)
Marketing started20231231
Package count2

External sources

Source: openFDA. Public-domain (CC0).