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venlafaxine hydrochloride, extended release

NDC 42799-962 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA209193
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (150 mg/1)
Marketing started20230315
Package count2

External sources

Source: openFDA. Public-domain (CC0).