NDC 68462-209
Moexipril Hydrochloride 7.5 mg tablet, film coated
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Moexiprilat: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 7.5 mg
- Approval
- ANDA ANDA090416
- On the market since
- Dec 31, 2010
- Package NDCs
68462-209-0168462-209-1068462-209-90- Official label
- DailyMed (National Library of Medicine), updated Jan 23, 2026
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