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

Is NDC 57377-0100-01 recalled?

Testo-100 Ciii

Yes — this exact package was recalled

1 FDA recall names the code 57377-0100-01 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.

1 of these recalls is still ongoing.

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 II · Moderate risk

Testo-100 Ciii

Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.

Ongoing Sterility / contamination Advanced Pharmaceutical Technology, Inc. NDC 57377-100-01 D-0258-2026

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