Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 62756-0142-02 recalled?

Metformin Hydrochloride · 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)

Yes — this exact package was recalled

4 FDA recalls name the code 62756-0142-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Metformin Hydrochloride
Strength
METFORMIN HYDROCHLORIDE 500 mg/1
Form
Tablet, Extended Release · Oral
Labeler
Sun Pharmaceutical Industries, Inc.
Type
Human Prescription Drug
Product code
62756-0142

Recalls naming this package

Class II · Moderate risk

Metformin Hydrochloride Extended Release Tablets

Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in one tablet.

Terminated Particulate / foreign matter Sun Pharmaceutical Industries, Inc. NDC 62756-142-02 D-0924-2018

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler