PLENVU (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE)
Summary
FDA approved PLENVU (POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE) by SALIX. NDA (New Drug) approval (Labeling) on 2023-09-08. FOR SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
NDA209381-13
Action Date
2023-09-08
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
PLENVU (generic: POLYETHYLENE GLYCOL 3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, ASCORBIC ACID, SODIUM ASCORBATE), FOR SOLUTION, ORAL. Application: NDA209381
Company
Context & Analysis
SALIX has 3 FDA actions in our database.
Frequently Asked Questions
How often does SALIX have FDA actions?
SALIX has 3 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 "NDA209381-13" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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