SUFLAVE (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, AND SODIUM CHLORIDE FOR ORA...
Summary
FDA approved SUFLAVE (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, AND SODIUM CHLORIDE FOR ORAL SOLUTION) by AZURITY. NDA (New Drug) approval (Type 4 - New Combination) on 2023-06-15. FOR SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
NDA215344-1
Action Date
2023-06-15
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
SUFLAVE (generic: POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, AND SODIUM CHLORIDE FOR ORAL SOLUTION), FOR SOLUTION, ORAL. Application: NDA215344
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 "NDA215344-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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