Glenmark Pharmaceuticals Limited
Goa, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 7 inspections on record, 1 with serious problems.
NDC 50436-6916
verapamil hydrochloride 120 mg tablet, film coated, extended release
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-292.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Recalls
- Mar 15, 2021 · Class II · Terminated
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 19205584
Product details
- Generic drug
- Verapamil: see every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 120 mg
- Approval
- ANDA ANDA090700
- On the market since
- Aug 5, 2011
- Package NDCs
50436-6916-1- Official label
- DailyMed (National Library of Medicine), updated Jun 11, 2018
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