SUTAB (SODIUM SULFATE, MAGNESIUM SULFATE, AND POTASSIUM CHLORIDE)
Summary
FDA approved SUTAB (SODIUM SULFATE, MAGNESIUM SULFATE, AND POTASSIUM CHLORIDE) by AZURITY. NDA (New Drug) approval (Labeling) on 2023-10-24. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA213135-4
Action Date
2023-10-24
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
SUTAB (generic: SODIUM SULFATE, MAGNESIUM SULFATE, AND POTASSIUM CHLORIDE), TABLET, ORAL. Application: NDA213135
Company
Context & Analysis
AZURITY has 21 FDA actions in our database.
Frequently Asked Questions
How often does AZURITY have FDA actions?
AZURITY has 21 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 "NDA213135-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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