NDC 42708-189
Meclizine Hydrochloride 25 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Amneal Pharmaceuticals's NDC 53746-442.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | No problems foundJul 19, 2024 · 6 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Meclizine: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA201451
- On the market since
- Apr 22, 2022
- Package NDCs
42708-189-30- Official label
- DailyMed (National Library of Medicine), updated May 11, 2026
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