FDA NDC Directory · JSON-LD · Markdown

Meclizine Hydrochloride

NDC 0904-7375 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA201451
Dosage form / routeTABLET · ORAL
Active ingredientsMECLIZINE HYDROCHLORIDE (12.5 mg/1)
Marketing started20220422
Package count1

External sources

Source: openFDA. Public-domain (CC0).