Product NDC: | 0409-7967 |
Proprietary Name: | Normosol-R |
Non Proprietary Name: | SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE |
Active Ingredient(s): | 30; 37; 222; 526; 502 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp; 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: | 0409-7967 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017586 |
Marketing Category: | NDA |
Start Marketing Date: | 20100920 |
Package NDC: | 0409-7967-03 |
Package Description: | 24 POUCH in 1 CASE (0409-7967-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
NDC Code | 0409-7967-03 |
Proprietary Name | Normosol-R |
Package Description | 24 POUCH in 1 CASE (0409-7967-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
Product NDC | 0409-7967 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM CHLORIDE, SODIUM ACETATE ANHYDROUS, SODIUM GLUCONATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100920 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE ANHYDROUS; SODIUM CHLORIDE; SODIUM GLUCONATE |
Strength Number | 30; 37; 222; 526; 502 |
Strength Unit | 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] |