NDC 67296-2138
Meclizine Hydrochloride 25 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 70710-1162.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Meclizine: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA213957
- On the market since
- Oct 29, 2020
- Package NDCs
67296-2138-3- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2026
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