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Desvenlafaxine Succinate

NDC 68180-604 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204172
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDESVENLAFAXINE SUCCINATE (25 mg/1)
Marketing started20220825
Package count1

External sources

Source: openFDA. Public-domain (CC0).