NDC 54868-5217

Metformin Hydrochloride 500 mg tablet, extended release

On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Sun Pharmaceutical Industries, Inc.'s NDC 62756-142.

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sun Pharmaceutical Industries, Inc. names for other drugs.

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Metformin: every company that makes it
Form
tablet, extended release
Strength
500 mg
Approval
ANDA ANDA077336
On the market since
Feb 9, 2006
Package NDCs
54868-5217-0 54868-5217-1 54868-5217-2 54868-5217-3 54868-5217-4 54868-5217-5
Official label
DailyMed (National Library of Medicine), updated May 6, 2015

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