Product NDC: | 0409-7998 |
Proprietary Name: | Potassium Chloride in Dextrose and Sodium Chloride |
Non Proprietary Name: | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
Active Ingredient(s): | 50; 1.49; 3 g/1000mL; g/1000mL; g/1000mL & nbsp; DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-7998 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018876 |
Marketing Category: | NDA |
Start Marketing Date: | 19860117 |
Package NDC: | 0409-7998-03 |
Package Description: | 24 POUCH in 1 CASE (0409-7998-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
NDC Code | 0409-7998-03 |
Proprietary Name | Potassium Chloride in Dextrose and Sodium Chloride |
Package Description | 24 POUCH in 1 CASE (0409-7998-03) > 1 BAG in 1 POUCH > 500 mL in 1 BAG |
Product NDC | 0409-7998 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19860117 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
Strength Number | 50; 1.49; 3 |
Strength Unit | g/1000mL; g/1000mL; g/1000mL |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |