FDA NDC Directory · JSON-LD · Markdown

Fulvestrant

NDC 71288-555 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA209714
Dosage form / routeINJECTION · INTRAMUSCULAR
Active ingredientsFULVESTRANT (50 mg/mL)
Marketing started20191121
Marketing ended20270131
Package count1

External sources

Source: openFDA. Public-domain (CC0).