| 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 |