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

Is NDC 84223-0002-04 recalled?

Tirzepatide · 60 mg in 1 VIAL (84223-002-04)

Yes — this exact package was recalled

1 FDA recall names the code 84223-0002-04 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.

2 of these recalls are still ongoing.

Active ingredient
Tirzepatide
Strength
TIRZEPATIDE 1 mg/mg
Form
Powder
Labeler
Nomida LLC
Type
Bulk Ingredient
Product code
84223-0002

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.

Other recalled products from this labeler