MPP Pharma LLC
Kansas City, MO, United States · makes it, tests it, packages it and labels it
Serious problems, FDA action Last FDA inspection Apr 2, 2026. 12 inspections on record, 4 with serious problems.
NDC 69367-412
Metformin Hydrochloride 500 mg tablet, film coated, extended release
On the label: Westminster Pharmaceuticals, LLC.
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 ANDA203832
- On the market since
- Oct 23, 2025
- Package NDCs
69367-412-60- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2025
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