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 |