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Desvenlafaxine

NDC 70436-012 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerSlate Run Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210014
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDESVENLAFAXINE SUCCINATE (50 mg/1)
Marketing started20200801
Package count2

External sources

Source: openFDA. Public-domain (CC0).