Product NDC: | 57826-426 |
Proprietary Name: | Haemonetics Anticoagulant Citrate Dextrose Solution |
Non Proprietary Name: | ANHYDROUS CITRIC ACID, TRISODIUM CITRATE DIHYDRATE, DEXTROSE MONOHYDRATE |
Active Ingredient(s): | 73; 245; 220 mg/mL; mg/mL; mg/mL & nbsp; ANHYDROUS CITRIC ACID, TRISODIUM CITRATE DIHYDRATE, DEXTROSE MONOHYDRATE |
Administration Route(s): | EXTRACORPOREAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57826-426 |
Labeler Name: | Haemonetics Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA980728 |
Marketing Category: | BLA |
Start Marketing Date: | 20130110 |
Package NDC: | 57826-426-04 |
Package Description: | 500 mL in 1 BAG (57826-426-04) |
NDC Code | 57826-426-04 |
Proprietary Name | Haemonetics Anticoagulant Citrate Dextrose Solution |
Package Description | 500 mL in 1 BAG (57826-426-04) |
Product NDC | 57826-426 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ANHYDROUS CITRIC ACID, TRISODIUM CITRATE DIHYDRATE, DEXTROSE MONOHYDRATE |
Dosage Form Name | SOLUTION |
Route Name | EXTRACORPOREAL |
Start Marketing Date | 20130110 |
Marketing Category Name | BLA |
Labeler Name | Haemonetics Corporation |
Substance Name | ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE |
Strength Number | 73; 245; 220 |
Strength Unit | mg/mL; mg/mL; mg/mL |
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] |