REDITREX
Summary
FDA approved REDITREX by NORDIC GRP. NDA (New Drug) approval (Labeling) on 2023-03-30. SOLUTION, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
NDA210737-2
Action Date
2023-03-30
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
REDITREX, SOLUTION, SUBCUTANEOUS. Application: NDA210737
Company
Context & Analysis
Frequently Asked Questions
How often does NORDIC GRP have FDA actions?
This is the only FDA action we have on record for NORDIC GRP in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA210737-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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