FDA NDC Directory · JSON-LD · Markdown

venlafaxine

NDC 70518-4168 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078932
Dosage form / routeTABLET · ORAL
Active ingredientsVENLAFAXINE HYDROCHLORIDE (75 mg/1)
Marketing started20240827
Package count1

External sources

Source: openFDA. Public-domain (CC0).