| 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] |