Class II ยท Moderate risk
Lupron Depot-Ped
Defective Delivery System: Some Lupron Depot Kits may contain a syringe with a potentially defective LuproLoc needle stick protection device.
National Drug Code
Is NDC 0074-3779-03 recalled?
Lupron Depot-PED · 1 KIT in 1 CARTON (0074-3779-03) * 1 SWAB in 1 PACKET * 1.5 mL in 1 SYRINGE
Yes — this exact package was recalled
1 FDA recall names the code 0074-3779-03 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
- leuprolide acetate
- Form
- Kit
- Labeler
- AbbVie Inc.
- Type
- Human Prescription Drug
- Product code
- 0074-3779
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
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