NDC Code | 23731-6051-5 |
Package Description | 12 BOTTLE, GLASS in 1 BOX (23731-6051-5) > 50 mL in 1 BOTTLE, GLASS |
Product NDC | 23731-6051 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Anticoagulant Citrate Dextrose A |
Non-Proprietary Name | Anhydrous Citric Acid, Dextrose Monohydrate, And Trisodium Citrate Dihydrate |
Dosage Form | SOLUTION |
Usage | EXTRACORPOREAL |
Start Marketing Date | 20030710 |
Marketing Category Name | NDA |
Application Number | BN020037 |
Manufacturer | Citra Labs |
Substance Name | ANHYDROUS CITRIC ACID; DEXTROSE MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE |
Strength | 7.3; 24.5; 22 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmacy Classes | Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] |