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

Is NDC 27437-0207-02 recalled?

Suprax

Yes — this exact package was recalled

1 FDA recall names the code 27437-0207-02 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.

This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.

Recalls naming this package

Class III · Low risk

Suprax

Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 27437-207-03 D-1187-2014
Class III · Low risk

Suprax

Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 27437-207-02 D-1186-2014

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.