Metformin ER Recall
Updated 10/10/20

The recall applies to metformin tablets, 500 mg ER and 750 mg ER,
sold under the brand name Time-Cap Labs, Inc.

The recalled tablets have either the number "101" or "102" on one side of the tablet,
and are plain on the other side.

The "NDC" codes for the recalled products can be entered in this FDA database:

NDC Database by "Selecting Type" NDC,
then enter the 10 digit numbers below for additional information.

Metformin Hydrochloride Extended-Release Tablets, USP 500mg:

90 counts: 49483-623-09

100 counts: 49483-623-01

500 counts: 49483-623-50

1000 counts: 49483-623-10

Metformin Hydrochloride Extended-Release Tablets, USP 750mg:

100 counts: 49483-624-01

Contact your pharmacist for inquiries regarding the Metformin ER you have at home.
We do not know what manufacturer or lot number was dispensed to you.

All pharmacies will be disposing of the recalled Metformin ER tablets
and won't dispense them to you.