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