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Meclizine Hydrochloride

NDC 70710-1162 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213957
Dosage form / routeTABLET · ORAL
Active ingredientsMECLIZINE HYDROCHLORIDE (25 mg/1)
Marketing started20201029
Package count5

External sources

Source: openFDA. Public-domain (CC0).