Cetrorelix Acetate

Meitheal Pharmaceuticals Inc.🇺🇸 United States

FDA Page

Effective Date: Sep 17, 2026
Approval ID: 9b3057ac-6cac-4509-a355-df76247b992c
Products: 0 registered
Version: 8

Regulatory Information

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Status

Approved

Full Title

Cetrorelix Acetate for Injection 0.25 mg(For Subcutaneous Use Only)

Quick Stats

Total Products0

Labelers1

Label Sections16

Regulatory Agency

🇺🇸

U.S. Food and Drug Administration

United States

Data Sources & Disclaimer: Approval information is sourced from official FDA databases. This content is for informational purposes only and does not constitute medical or regulatory advice. Always refer to official FDA websites for the most current information.