CPDA-1 - 0942-6321-04 - (Anticoagulant Citrate Phosphate Dextrose Adenine)

Alphabetical Index


Drug Information of CPDA-1

Product NDC: 0942-6321
Proprietary Name: CPDA-1
Non Proprietary Name: Anticoagulant Citrate Phosphate Dextrose Adenine
Active Ingredient(s): 9.6; 105; 1.12; 78; 921    mg/35mL; mg/35mL; g/35mL; mg/35mL; mg/35mL & nbsp;   Anticoagulant Citrate Phosphate Dextrose Adenine
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CPDA-1

Product NDC: 0942-6321
Labeler Name: Fenwal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BN770420
Marketing Category: NDA
Start Marketing Date: 20070601

Package Information of CPDA-1

Package NDC: 0942-6321-04
Package Description: 35 mL in 1 BAG (0942-6321-04)

NDC Information of CPDA-1

NDC Code 0942-6321-04
Proprietary Name CPDA-1
Package Description 35 mL in 1 BAG (0942-6321-04)
Product NDC 0942-6321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Anticoagulant Citrate Phosphate Dextrose Adenine
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070601
Marketing Category Name NDA
Labeler Name Fenwal, Inc.
Substance Name ADENINE; ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE
Strength Number 9.6; 105; 1.12; 78; 921
Strength Unit mg/35mL; mg/35mL; g/35mL; mg/35mL; mg/35mL
Pharmaceutical Classes Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]

Complete Information of CPDA-1


General Information