NDC 71335-1872

Meclizine Hydrochloride 12.5 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-660.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Meclizine: every company that makes it
Form
tablet, oral
Strength
12.5 mg
Approval
NDA authorized generic NDA010721
On the market since
Jan 15, 2020
Package NDCs
71335-1872-1 71335-1872-2 71335-1872-3 71335-1872-4 71335-1872-5 71335-1872-6 71335-1872-7 71335-1872-8
Official label
DailyMed (National Library of Medicine), updated Aug 20, 2025

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