NDC 69367-181

Metformin Hydrochloride 850 mg tablet, film coated

On the label: Westminster Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Metformin: every company that makes it
Form
tablet, film coated, oral
Strength
850 mg
Approval
ANDA ANDA203769
On the market since
Nov 21, 2017
Package NDCs
69367-181-01 69367-181-05
Official label
DailyMed (National Library of Medicine), updated May 22, 2026

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