NDC 68071-2380

Meclizine Hydrochloride 25 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-661.

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
25 mg
Approval
NDA authorized generic NDA010721
On the market since
Jan 15, 2020
Package NDCs
68071-2380-2 68071-2380-3 68071-2380-9
Official label
DailyMed (National Library of Medicine), updated Mar 2, 2026

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