NDC 68071-2398

Metformin Hydrochloride 1000 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-107.

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
1000 mg
Approval
ANDA ANDA203769
On the market since
Feb 1, 2015
Package NDCs
68071-2398-2 68071-2398-3 68071-2398-6 68071-2398-8 68071-2398-9
Official label
DailyMed (National Library of Medicine), updated May 12, 2021

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