EXBLIFEP
Summary
FDA approved EXBLIFEP by ORCHID PHARMA. NDA (New Drug) approval (Type 1 - New Molecular Entity and Type 4 - New Combination) on 2024-02-22. POWDER, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA216165-1
Action Date
2024-02-22
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
EXBLIFEP, POWDER, INTRAVENOUS. Application: NDA216165
Company
Context & Analysis
Frequently Asked Questions
How often does ORCHID PHARMA have FDA actions?
This is the only FDA action we have on record for ORCHID PHARMA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA216165-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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