NDC 70934-830

Metformin Hydrochloride 1000 mg tablet

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's a repackaged product: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Granules Pharmaceuticals Inc.'s NDC 70010-065.

Where the pills inside were made

Granules India Limited

Medchal-Malkajgiri District, India · makes it, tests it, packages it and labels it

Problems found, fixed voluntarily Last FDA inspection Feb 14, 2020. 6 inspections on record.

Granules Life Sciences Private Limited

Shameerpet Medchal-Malkajgiri, India · makes it, tests it, packages it and labels it

Problems found, fixed voluntarily Last FDA inspection Dec 19, 2025. 1 inspection on record.

Repackaging site

Product details

Generic drug
Metformin: see every company that makes it
Form
tablet
Strength
1000 mg
Approval
ANDA ANDA090564
On the market since
Feb 25, 2021
Package NDCs
70934-830-90
Official label
DailyMed (National Library of Medicine), updated Feb 26, 2021

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