Glenmark Pharmaceuticals Limited
Dhar, India · makes it and tests it
Serious problems, FDA action Last FDA inspection Feb 14, 2025. 8 inspections on record, 1 with serious problems.
NDC 68462-520
Metformin Hydrochloride 500 mg tablet, film coated, extended release
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
Product details
- Generic drug
- Metformin: see every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA212969
- On the market since
- Nov 25, 2019
- Package NDCs
68462-520-0168462-520-0568462-520-10- Official label
- DailyMed (National Library of Medicine), updated Sep 23, 2026
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