| Product ID | 0942-9005_26a93e4e-50c7-42d2-b169-c3ce9a89d106 |
| NDC | 0942-9005 |
| Product Type | Human Prescription Drug |
| Proprietary Name | ACD-A |
| Generic Name | Antiocoagulant Citrate Dextrose Solution, Formula A |
| Dosage Form | Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2012-10-24 |
| Marketing Category | NDA / NDA |
| Application Number | BN160918 |
| Labeler Name | Fenwal, Inc. |
| Substance Name | ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; SODIUM CITRATE, UNSPECIFIED FORM |
| Active Ingredient Strength | 730 mg/100mL; g/100mL; g/100mL |
| Pharm Classes | Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |