NDC 60687-775
Meclizine Hydrochloride 12.5 mg tablet
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Amneal Pharmaceuticals's NDC 53746-441.
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
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Mar 16, 2026 · Class II · Amerisource Health Services LLC
Failed tablet specifications.
Lots: Lot #1024852; Exp 9/30/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Meclizine: every company that makes it
- Form
- tablet, oral
- Strength
- 12.5 mg
- Approval
- ANDA ANDA201451
- On the market since
- Sep 8, 2023
- Package NDCs
60687-775-0160687-775-1160687-775-65- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2025
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