InterSol - 0942-9601-12 - (Platelet Additive 3)

Alphabetical Index


Drug Information of InterSol

Product NDC: 0942-9601
Proprietary Name: InterSol
Non Proprietary Name: Platelet Additive 3
Active Ingredient(s): 2.21; 2.26; 1.53; .465; 1.59    g/500mL; g/500mL; g/500mL; g/500mL; g/500mL & nbsp;   Platelet Additive 3
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of InterSol

Product NDC: 0942-9601
Labeler Name: Fenwal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BN080041
Marketing Category: NDA
Start Marketing Date: 20121025

Package Information of InterSol

Package NDC: 0942-9601-12
Package Description: 500 mL in 1 BAG (0942-9601-12)

NDC Information of InterSol

NDC Code 0942-9601-12
Proprietary Name InterSol
Package Description 500 mL in 1 BAG (0942-9601-12)
Product NDC 0942-9601
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Platelet Additive 3
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20121025
Marketing Category Name NDA
Labeler Name Fenwal, Inc.
Substance Name SODIUM ACETATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE
Strength Number 2.21; 2.26; 1.53; .465; 1.59
Strength Unit g/500mL; g/500mL; g/500mL; g/500mL; g/500mL
Pharmaceutical Classes Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]

Complete Information of InterSol


General Information