Home > National Drug Code (NDC) > LEUKOSEP - SOLX A ADDITIVE SOLUTION

LEUKOSEP - SOLX A ADDITIVE SOLUTION - 53157-303-03 - (SOL A ADDITIVE SOLUTION)

Alphabetical Index


Drug Information of LEUKOSEP - SOLX A ADDITIVE SOLUTION

Product NDC: 53157-303
Proprietary Name: LEUKOSEP - SOLX A ADDITIVE SOLUTION
Non Proprietary Name: SOL A ADDITIVE SOLUTION
Active Ingredient(s): 30; 1.1    mg/80mL; g/80mL & nbsp;   SOL A ADDITIVE SOLUTION
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of LEUKOSEP - SOLX A ADDITIVE SOLUTION

Product NDC: 53157-303
Labeler Name: Haemonetics Manufacturing Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA110059
Marketing Category: NDA
Start Marketing Date: 20130515

Package Information of LEUKOSEP - SOLX A ADDITIVE SOLUTION

Package NDC: 53157-303-03
Package Description: 80 mL in 1 BAG (53157-303-03)

NDC Information of LEUKOSEP - SOLX A ADDITIVE SOLUTION

NDC Code 53157-303-03
Proprietary Name LEUKOSEP - SOLX A ADDITIVE SOLUTION
Package Description 80 mL in 1 BAG (53157-303-03)
Product NDC 53157-303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SOL A ADDITIVE SOLUTION
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130515
Marketing Category Name NDA
Labeler Name Haemonetics Manufacturing Inc
Substance Name ADENINE; MANNITOL
Strength Number 30; 1.1
Strength Unit mg/80mL; g/80mL
Pharmaceutical Classes Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC]

Complete Information of LEUKOSEP - SOLX A ADDITIVE SOLUTION


General Information