NDC Code | 0338-9669-01 |
Package Description | 250 mL in 1 BAG (0338-9669-01) |
Product NDC | 0338-9669 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Anticoagulant Sodium Citrate |
Non-Proprietary Name | Trisodium Citrate Dihydrate |
Dosage Form | SOLUTION |
Usage | EXTRACORPOREAL |
Start Marketing Date | 20240402 |
Marketing Category Name | NDA |
Application Number | BN980123 |
Manufacturer | Baxter Healthcare Corporation |
Substance Name | TRISODIUM CITRATE DIHYDRATE |
Strength | 40 |
Strength Unit | mg/mL |
Pharmacy Classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |