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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 217569


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NDA 217569 describes VASOPRESSIN IN SODIUM CHLORIDE 0.9%, which is a drug marketed by Baxter Hlthcare Corp and Long Grove Pharms and is included in two NDAs. It is available from two suppliers. Additional details are available on the VASOPRESSIN IN SODIUM CHLORIDE 0.9% profile page.

The generic ingredient in VASOPRESSIN IN SODIUM CHLORIDE 0.9% is vasopressin. There are nine drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the vasopressin profile page.
Summary for 217569
Tradename:VASOPRESSIN IN SODIUM CHLORIDE 0.9%
Applicant:Baxter Hlthcare Corp
Ingredient:vasopressin
Patents:0
Pharmacology for NDA: 217569
Physiological EffectDecreased Diuresis
Vasoconstriction
Suppliers and Packaging for NDA: 217569
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
VASOPRESSIN IN SODIUM CHLORIDE 0.9% vasopressin SOLUTION;INTRAVENOUS 217569 NDA Baxter Healthcare Corporation 0338-9640 0338-9640-12 12 BAG in 1 CARTON (0338-9640-12) / 100 mL in 1 BAG
VASOPRESSIN IN SODIUM CHLORIDE 0.9% vasopressin SOLUTION;INTRAVENOUS 217569 NDA Baxter Healthcare Corporation 0338-9647 0338-9647-12 12 BAG in 1 CARTON (0338-9647-12) / 100 mL in 1 BAG

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:SOLUTION;INTRAVENOUSStrength20UNITS/100ML (0.2UNITS/ML)
Approval Date:Sep 29, 2023TE:RLD:Yes

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:SOLUTION;INTRAVENOUSStrength40UNITS/100ML (0.4UNITS/ML)
Approval Date:Sep 29, 2023TE:RLD:Yes

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