Inventia Healthcare Limited
Thane, India · makes it, tests it, packages it and labels it
Problems found, fixed voluntarily Last FDA inspection Feb 12, 2025. 4 inspections on record.
NDC 42708-201
Metformin Hydrochloride 500 mg tablet, extended release
On the label: QPharma, Inc..
It's a repackaged product: QPharma, Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-159.
Where the pills inside were made
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Metformin: see every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA201991
- On the market since
- Mar 1, 2013
- Package NDCs
42708-201-60- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2026
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