MICAFUNGIN IN SODIUM CHLORIDE
Summary
FDA approved MICAFUNGIN IN SODIUM CHLORIDE by BAXTER HLTHCARE CORP. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2023-09-29. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA216142-1
Action Date
2023-09-29
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
MICAFUNGIN IN SODIUM CHLORIDE, SOLUTION, INTRAVENOUS. Application: NDA216142
Company
Context & Analysis
BAXTER HLTHCARE CORP has 15 FDA actions in our database.
Frequently Asked Questions
How often does BAXTER HLTHCARE CORP have FDA actions?
BAXTER HLTHCARE CORP has 15 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 "NDA216142-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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