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Fluvoxamine maleate

NDC 69452-287 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217917
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUVOXAMINE MALEATE (25 mg/1)
Marketing started20240523
Package count1

External sources

Source: openFDA. Public-domain (CC0).