| 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] |