NDC 67296-2250
Meclizine Hydrochloride 12.5 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-807.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 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
- 12.5 mg
- Approval
- ANDA ANDA202640
- On the market since
- Sep 14, 2023
- Package NDCs
67296-2250-3- Official label
- DailyMed (National Library of Medicine), updated May 29, 2026
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