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Desvenlafaxine

NDC 0054-0400 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204083
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDESVENLAFAXINE SUCCINATE (50 mg/1)
Marketing started20170301
Package count2

External sources

Source: openFDA. Public-domain (CC0).