Class II ยท Moderate risk
Cetrotide (cetrorelix acetate for Injection)
Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.
National Drug Code
Is NDC 44087-1225-01 recalled?
Cetrotide · 1 KIT in 1 CARTON (44087-1225-1) * 1 mL in 1 VIAL, GLASS * 1 mL in 1 SYRINGE, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 44087-1225-01 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.
- Active ingredient
- cetrorelix acetate
- Form
- Kit · Subcutaneous
- Labeler
- EMD Serono, Inc.
- Type
- Human Prescription Drug
- Product code
- 44087-1225
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.
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