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Fluoxetine

NDC 65862-194 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20080131
Marketing ended20280229
Package count4

External sources

Source: openFDA. Public-domain (CC0).