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Fluoxetine

NDC 0615-8612 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20250711
Package count2

External sources

Source: openFDA. Public-domain (CC0).