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MECLIZINE HYDROCHLORIDE

NDC 59651-809 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMECLIZINE
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202640
Dosage form / routeTABLET · ORAL
Active ingredientsMECLIZINE HYDROCHLORIDE (50 mg/1)
Marketing started20230914
Package count2

External sources

Source: openFDA. Public-domain (CC0).