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Meclizine Hydrochloride

NDC 53746-441 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201451
Dosage form / routeTABLET · ORAL
Active ingredientsMECLIZINE HYDROCHLORIDE (12.5 mg/1)
Marketing started20220422
Package count2

External sources

Source: openFDA. Public-domain (CC0).