NDC 71335-3139
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.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
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
71335-3139-1- Official label
- DailyMed (National Library of Medicine), updated May 27, 2026
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