| NDC Code | 0942-9605-01 |
|---|
| Package Description | 800 mL in 1 BAG (0942-9605-01) |
|---|
| Product NDC | 0942-9605 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Intersol |
|---|
| Non-Proprietary Name | Platelet Additive 3 |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20250414 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | BN080041 |
|---|
| Manufacturer | Fenwal, Inc. |
|---|
| Substance Name | SODIUM ACETATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM; 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] |
|---|