Product NDC: | 0338-0675 |
Proprietary Name: | Potassium Chloride in Dextrose and Sodium Chloride |
Non Proprietary Name: | Potassium Chloride, Dextrose Monohydrate and Sodium Chloride |
Active Ingredient(s): | 5; 300; 450 g/100mL; mg/100mL; mg/100mL & nbsp; Potassium Chloride, Dextrose Monohydrate and Sodium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0338-0675 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018008 |
Marketing Category: | NDA |
Start Marketing Date: | 19790202 |
Package NDC: | 0338-0675-04 |
Package Description: | 1000 mL in 1 BAG (0338-0675-04) |
NDC Code | 0338-0675-04 |
Proprietary Name | Potassium Chloride in Dextrose and Sodium Chloride |
Package Description | 1000 mL in 1 BAG (0338-0675-04) |
Product NDC | 0338-0675 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Potassium Chloride, Dextrose Monohydrate and Sodium Chloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19790202 |
Marketing Category Name | NDA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
Strength Number | 5; 300; 450 |
Strength Unit | g/100mL; mg/100mL; mg/100mL |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |