| Product NDC: | 53157-303 |
| Proprietary Name: | LEUKOSEP - SOLX A ADDITIVE SOLUTION |
| Non Proprietary Name: | SOL A ADDITIVE SOLUTION |
| Active Ingredient(s): | 30; 1.1 mg/80mL; g/80mL & nbsp; SOL A ADDITIVE SOLUTION |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53157-303 |
| Labeler Name: | Haemonetics Manufacturing Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA110059 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130515 |
| Package NDC: | 53157-303-03 |
| Package Description: | 80 mL in 1 BAG (53157-303-03) |
| NDC Code | 53157-303-03 |
| Proprietary Name | LEUKOSEP - SOLX A ADDITIVE SOLUTION |
| Package Description | 80 mL in 1 BAG (53157-303-03) |
| Product NDC | 53157-303 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SOL A ADDITIVE SOLUTION |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20130515 |
| Marketing Category Name | NDA |
| Labeler Name | Haemonetics Manufacturing Inc |
| Substance Name | ADENINE; MANNITOL |
| Strength Number | 30; 1.1 |
| Strength Unit | mg/80mL; g/80mL |
| Pharmaceutical Classes | Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC] |