NDC 68788-4170
Meclizine Hydrochloride 25 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Aurobindo Pharma Limited's NDC 59651-808.
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
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Meclizine: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA202640
- On the market since
- Aug 3, 2026
- Package NDCs
68788-4170-168788-4170-3- Official label
- DailyMed (National Library of Medicine), updated Aug 3, 2026
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