Class III ยท Low risk
Menopur 75 IU
Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chloride, USP
National Drug Code
Is NDC 55566-7501-02 recalled?
Menopur · 1 CARTON in 1 CARTON (55566-7501-2) / 1 KIT in 1 CARTON (55566-7501-1) * 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55566-7502-0) * 1 INJECTION in 1 VIAL (55566-1600-0
Yes — this exact package was recalled
1 FDA recall names the code 55566-7501-02 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
- menotropins
- Form
- Kit
- Labeler
- Ferring Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 55566-7501
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
- 55566-6500 Endometrin 2
- 55566-1000 See recall 1
- 55566-1010 Fyremadel 1
- 55566-1501 See recall 1
- 55566-2500 See recall 1
- 55566-8303 Firmagon 1
Free recall alerts
Know the day your medication is recalled
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