CETRORELIX ACETATE
Summary
FDA approved CETRORELIX ACETATE by TEVA PHARMS INC. ANDA (Generic) approval (Labeling) on 2025-11-06. POWDER, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
ANDA215737-3
Action Date
2025-11-06
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
CETRORELIX ACETATE, POWDER, SUBCUTANEOUS. Application: ANDA215737
Company
Context & Analysis
TEVA PHARMS INC has 7 FDA actions in our database.
Frequently Asked Questions
How often does TEVA PHARMS INC have FDA actions?
TEVA PHARMS INC has 7 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA215737-3" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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