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Fluoxetine

NDC 46708-271 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090223
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (10 mg/1)
Marketing started20090701
Package count4

External sources

Source: openFDA. Public-domain (CC0).