FDA NDC Directory · JSON-LD · Markdown

Meclizine Hydrochloride

NDC 65162-442 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201451
Dosage form / routeTABLET · ORAL
Active ingredientsMECLIZINE HYDROCHLORIDE (25 mg/1)
Marketing started20100212
Package count5

External sources

Source: openFDA. Public-domain (CC0).