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Fluvoxamine maleate

NDC 0832-1671 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075888
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUVOXAMINE MALEATE (50 mg/1)
Marketing started20001129
Marketing ended20260630
Package count0

External sources

Source: openFDA. Public-domain (CC0).