CPD - 0942-9206-01 - (Anticoagulant Citrate Phosphate Dextrose (CPD))

Alphabetical Index


Drug Information of CPD

Product NDC: 0942-9206
Proprietary Name: CPD
Non Proprietary Name: Anticoagulant Citrate Phosphate Dextrose (CPD)
Active Ingredient(s): 188; 1.61; 140; 1.66    mg/63mL; g/63mL; mg/63mL; g/63mL & nbsp;   Anticoagulant Citrate Phosphate Dextrose (CPD)
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CPD

Product NDC: 0942-9206
Labeler Name: Fenwal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BN170401
Marketing Category: NDA
Start Marketing Date: 20070301

Package Information of CPD

Package NDC: 0942-9206-01
Package Description: 63 mL in 1 BAG (0942-9206-01)

NDC Information of CPD

NDC Code 0942-9206-01
Proprietary Name CPD
Package Description 63 mL in 1 BAG (0942-9206-01)
Product NDC 0942-9206
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Anticoagulant Citrate Phosphate Dextrose (CPD)
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070301
Marketing Category Name NDA
Labeler Name Fenwal, Inc.
Substance Name ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE
Strength Number 188; 1.61; 140; 1.66
Strength Unit mg/63mL; g/63mL; mg/63mL; g/63mL
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 CPD


General Information