COPAXONE (GLATIRAMER ACETATE)
Summary
FDA approved COPAXONE (GLATIRAMER ACETATE) by TEVA PHARMS USA. NDA (New Drug) approval (Labeling) on 2026-06-22. INJECTABLE, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
NDA020622-121
Action Date
2026-06-22
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
COPAXONE (generic: GLATIRAMER ACETATE), INJECTABLE, SUBCUTANEOUS. Application: NDA020622
Company
Context & Analysis
TEVA PHARMS USA has 39 FDA actions in our database.
Frequently Asked Questions
How often does TEVA PHARMS USA have FDA actions?
TEVA PHARMS USA has 39 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 "NDA020622-121" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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