NDC 68071-2386

Metformin Hydrochloride 500 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-105.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Metformin: every company that makes it
Form
tablet
Strength
500 mg
Approval
ANDA ANDA203769
On the market since
Feb 1, 2015
Package NDCs
68071-2386-1 68071-2386-2 68071-2386-3 68071-2386-6 68071-2386-9
Official label
DailyMed (National Library of Medicine), updated Apr 13, 2021

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