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] |