NDC Code | 0942-9602-12 |
Package Description | 500 mL in 1 BAG (0942-9602-12) |
Product NDC | 0942-9602 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Intersol |
Non-Proprietary Name | Platelet Additive 3 |
Dosage Form | SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20190605 |
Marketing Category Name | NDA |
Application Number | BN080041 |
Manufacturer | Fenwal, Inc. |
Substance Name | SODIUM ACETATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC; SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE |
Strength | 442; 452; 305; 93; 318 |
Strength Unit | mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL |
Pharmacy Classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |