NDC 68462-260
verapamil hydrochloride 240 mg tablet, film coated, extended release
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 |
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 19205584
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Verapamil: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 240 mg
- Approval
- ANDA ANDA078906
- On the market since
- Sep 17, 2009
- Package NDCs
68462-260-0168462-260-0568462-260-1068462-260-3068462-260-90- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
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