NDC 71288-558

Cetrorelix Acetate 0.25 mg per 2 mL kit

On the label: Meitheal Pharmaceuticals Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Meitheal Pharmaceuticals Inc. names for other drugs.

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Cetrorelix: every company that makes it
Form
kit, subcutaneous
Strength
0.25 mg per 2 mL
Approval
ANDA ANDA214540
On the market since
Apr 24, 2024
Package NDCs
71288-556-02 71288-557-81 71288-558-90
Official label
DailyMed (National Library of Medicine), updated Sep 17, 2026

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