NDC 51655-649

Metformin Hydrochloride 1000 mg tablet, film coated

On the label: Northwind Pharmaceuticals. It's a repackaged product: Northwind Pharmaceuticals rebottles it from Aurobindo Pharma Limited's NDC 65862-010.

Where the pills inside were made

Aurobindo Pharma Limited

Medchal, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.

Aurobindo Pharma Limited

Mahabubnagar, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection May 10, 2022. 7 inspections on record, 1 with serious problems.

Repackaging site

Recalls

Product details

Generic drug
Metformin: see every company that makes it
Form
tablet, film coated, oral
Strength
1000 mg
Approval
ANDA ANDA077095
On the market since
Apr 1, 2021
Package NDCs
51655-649-25 51655-649-26 51655-649-52
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2026

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