NDC 51655-644

Metformin Hydrochloride 1000 mg tablet, film coated

On the label: Northwind Pharmaceuticals. It's a repackaged product: Northwind Pharmaceuticals rebottles it from Laurus Labs Limited's NDC 42385-949.

Where the pills inside were made

Laurus Labs Limited

Anakapalli, India · makes it, makes the active ingredient and tests it

Problems found, fixed voluntarily Last FDA inspection Feb 10, 2023. 2 inspections on record.

Repackaging site

Product details

Generic drug
Metformin: see every company that makes it
Form
tablet, film coated, oral
Strength
1000 mg
Approval
ANDA ANDA209882
On the market since
Jul 6, 2023
Package NDCs
51655-644-26
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?