Product NDC: | 0942-9001 |
Proprietary Name: | ACD Blood-Pack Units (PL 146 Plastic) |
Non Proprietary Name: | Anticoagulant Citrate Dextrose (ACD) |
Active Ingredient(s): | 493; 1.65; 1.48 mg/67.5mL; g/67.5mL; g/67.5mL & nbsp; Anticoagulant Citrate Dextrose (ACD) |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0942-9001 |
Labeler Name: | Fenwal, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BN160918 |
Marketing Category: | NDA |
Start Marketing Date: | 20070301 |
Package NDC: | 0942-9001-01 |
Package Description: | 67.5 mL in 1 BAG (0942-9001-01) |
NDC Code | 0942-9001-01 |
Proprietary Name | ACD Blood-Pack Units (PL 146 Plastic) |
Package Description | 67.5 mL in 1 BAG (0942-9001-01) |
Product NDC | 0942-9001 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Anticoagulant Citrate Dextrose (ACD) |
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; TRISODIUM CITRATE DIHYDRATE |
Strength Number | 493; 1.65; 1.48 |
Strength Unit | mg/67.5mL; g/67.5mL; g/67.5mL |
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] |