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

Is NDC 49281-0752-21 recalled?

Tubersol · 1 VIAL, MULTI-DOSE in 1 CARTON (49281-752-21) / 1 mL in 1 VIAL, MULTI-DOSE (49281-752-78)

Yes — this exact package was recalled

1 FDA recall names the code 49281-0752-21 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
Tuberculin Purified Protein Derivative
Strength
TUBERCULIN PURIFIED PROTEIN DERIVATIVE 5 [iU]/.1mL
Form
Injection, Solution · Intradermal
Labeler
Sanofi Vaccines US Inc.
Type
Human Prescription Drug
Product code
49281-0752

Recalls naming this package

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.