NDC 69367-182

Metformin Hydrochloride 1000 mg tablet, film coated

On the label: Westminster Pharmaceuticals, LLC.

Where it's made

ScieGen Pharmaceuticals, INC.

Hauppauge, NY, United States · makes it, tests it, packages it and labels it

Problems found, fixed voluntarily Last FDA inspection May 15, 2026. 15 inspections on record, 1 with serious problems.

Product details

Generic drug
Metformin: see every company that makes it
Form
tablet, film coated, oral
Strength
1000 mg
Approval
ANDA ANDA203769
On the market since
Nov 21, 2017
Package NDCs
69367-182-01 69367-182-05 69367-182-10
Official label
DailyMed (National Library of Medicine), updated May 22, 2026

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