KENALOG-10 (TRIAMCINOLONE ACETONIDE)
Summary
FDA approved KENALOG-10 (TRIAMCINOLONE ACETONIDE) by APOTHECON. NDA (New Drug) approval (Manufacturing (CMC)) on 2024-08-14. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
NDA012041-52
Action Date
2024-08-14
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
KENALOG-10 (generic: TRIAMCINOLONE ACETONIDE), INJECTABLE, INJECTION. Application: NDA012041
Company
Context & Analysis
APOTHECON has 2 FDA actions in our database.
Frequently Asked Questions
How often does APOTHECON have FDA actions?
APOTHECON 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 "NDA012041-52" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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