E-Z-DISK (BARIUM SULFATE)
Summary
FDA approved E-Z-DISK (BARIUM SULFATE) by BRACCO. NDA (New Drug) approval (Type 7 - Drug Already Marketed without Approved NDA) on 2025-08-01. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA219840-1
Action Date
2025-08-01
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
E-Z-DISK (generic: BARIUM SULFATE), TABLET, ORAL. Application: NDA219840
Company
Context & Analysis
BRACCO has 7 FDA actions in our database.
Frequently Asked Questions
How often does BRACCO have FDA actions?
BRACCO has 7 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 "NDA219840-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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