ACTHAR (REPOSITORY CORTICOTROPIN)
Summary
FDA approved ACTHAR (REPOSITORY CORTICOTROPIN) by MALLINCKRODT IRELAND. NDA (New Drug) approval (Labeling) on 2024-02-29. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
NDA008372-74
Action Date
2024-02-29
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ACTHAR (generic: REPOSITORY CORTICOTROPIN), INJECTABLE, INJECTION. Application: NDA008372
Company
Context & Analysis
MALLINCKRODT IRELAND has 2 FDA actions in our database.
Frequently Asked Questions
How often does MALLINCKRODT IRELAND have FDA actions?
MALLINCKRODT IRELAND has 2 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 "NDA008372-74" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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