NDC 53808-0936
verapamil hydrochloride 120 mg tablet, film coated, extended release
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-292.
Where the pills inside were 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 |
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
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
- Strength
- 120 mg
- Approval
- ANDA ANDA090700
- On the market since
- Jan 1, 2014
- Package NDCs
53808-0936-1- Official label
- DailyMed (National Library of Medicine), updated Mar 7, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?