VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN)
Summary
FDA approved VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN) by LONG GROVE PHARMS. NDA (New Drug) approval (Type 3 - New Dosage Form) on 2024-07-11. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA217766-1
Action Date
2024-07-11
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
VASOPRESSIN IN 0.9% SODIUM CHLORIDE (generic: VASOPRESSIN), SOLUTION, INTRAVENOUS. Application: NDA217766
Company
Context & Analysis
LONG GROVE PHARMS has 6 FDA actions in our database.
Frequently Asked Questions
How often does LONG GROVE PHARMS have FDA actions?
LONG GROVE PHARMS has 6 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 "NDA217766-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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