Class II · Moderate risk
Trulicity (dulaglutide)
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
National Drug Code
Is NDC 0002-1433-80 recalled?
Trulicity · 4 SYRINGE in 1 CARTON (0002-1433-80) / .5 mL in 1 SYRINGE (0002-1433-01)
Yes — this exact package was recalled
2 FDA recalls name the code 0002-1433-80 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
- Dulaglutide
- Strength
- DULAGLUTIDE .75 mg/.5mL
- Form
- Injection, Solution · Subcutaneous
- Labeler
- Eli Lilly and Company
- Type
- Human Prescription Drug
- Product code
- 0002-1433
Recalls naming this package
Class II · Moderate risk
Trulicity (dulaglutide)
Labeling: Label error on declared strength - autoinjector devices labeled as 0.75 mg / 0.5 mL actually contain 1.5 mg / 0.5 mL of product.
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
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