FDA NDC Directory · JSON-LD · Markdown

MECLIZINE HYDROCHLORIDE

NDC 23155-943 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMECLIZINE
Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205136
Dosage form / routeTABLET · ORAL
Active ingredientsMECLIZINE HYDROCHLORIDE (50 mg/1)
Marketing started20260625
Package count2

External sources

Source: openFDA. Public-domain (CC0).