Product NDC: | 0409-7968 |
Proprietary Name: | Normosol-R and Dextrose |
Non Proprietary Name: | Dextrose, Sodium Chloride, Sodium Acetate Anhydrous, Sodium Gluconate, Potassium Chloride, and Magnesium Chloride |
Active Ingredient(s): | 5; 30; 37; 222; 526; 502 g/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp; Dextrose, Sodium Chloride, Sodium Acetate Anhydrous, Sodium Gluconate, Potassium Chloride, and Magnesium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-7968 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017609 |
Marketing Category: | NDA |
Start Marketing Date: | 20100916 |
Package NDC: | 0409-7968-09 |
Package Description: | 12 BAG in 1 CASE (0409-7968-09) > 1000 mL in 1 BAG |
NDC Code | 0409-7968-09 |
Proprietary Name | Normosol-R and Dextrose |
Package Description | 12 BAG in 1 CASE (0409-7968-09) > 1000 mL in 1 BAG |
Product NDC | 0409-7968 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dextrose, Sodium Chloride, Sodium Acetate Anhydrous, Sodium Gluconate, Potassium Chloride, and Magnesium Chloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100916 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | DEXTROSE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE ANHYDROUS; SODIUM CHLORIDE; SODIUM GLUCONATE |
Strength Number | 5; 30; 37; 222; 526; 502 |
Strength Unit | g/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |