ACD-A is a Intravenous Solution in the Human Prescription Drug category. It is labeled and distributed by Fenwal, Inc.. The primary component is Dextrose Monohydrate; Sodium Citrate; Anhydrous Citric Acid.
Product ID | 0942-0641_0117e68c-08df-40f0-9e1f-aeb50ce17a6e |
NDC | 0942-0641 |
Product Type | Human Prescription Drug |
Proprietary Name | ACD-A |
Generic Name | Anticoagulant Citrate Dextrose Solution Formula A |
Dosage Form | Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2007-03-01 |
Marketing Category | NDA / NDA |
Application Number | BN160918 |
Labeler Name | Fenwal, Inc. |
Substance Name | DEXTROSE MONOHYDRATE; SODIUM CITRATE; ANHYDROUS CITRIC ACID |
Active Ingredient Strength | 12 g/500mL; g/500mL; g/500mL |
Pharm 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] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2007-03-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | BN160918 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2007-03-01 |
Marketing Category | NDA |
Application Number | BN160918 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2007-03-01 |
Ingredient | Strength |
---|---|
DEXTROSE MONOHYDRATE | 12.25 g/500mL |
SPL SET ID: | 22805f0d-ba58-41ea-b245-19980abcda22 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
0942-0641 | ACD-A | Anticoagulant Citrate Dextrose Solution Formula A |
0942-9005 | ACD-A | Antiocoagulant Citrate Dextrose Solution, Formula A |
53157-796 | ACD-A | Anticoagulant Citrate Dextrose Solution A |