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Potassium Chloride in Dextrose and Sodium Chloride
Potassium Chloride in Dextrose and Sodium Chloride - 0338-0671-03 - (Potassium Chloride, Dextrose Monohydrate and Sodium Chloride)
Drug Information of Potassium Chloride in Dextrose and Sodium Chloride
| Product NDC: | 0338-0671 |
| Proprietary Name: | Potassium Chloride in Dextrose and Sodium Chloride |
| Non Proprietary Name: | Potassium Chloride, Dextrose Monohydrate and Sodium Chloride |
| Active Ingredient(s): | 5; 150; 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) |
Labeler Information of Potassium Chloride in Dextrose and Sodium Chloride
| Product NDC: | 0338-0671 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018008 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19790202 |
Package Information of Potassium Chloride in Dextrose and Sodium Chloride
| Package NDC: | 0338-0671-03 |
| Package Description: | 500 mL in 1 BAG (0338-0671-03) |
NDC Information of Potassium Chloride in Dextrose and Sodium Chloride
| NDC Code | 0338-0671-03 |
| Proprietary Name | Potassium Chloride in Dextrose and Sodium Chloride |
| Package Description | 500 mL in 1 BAG (0338-0671-03) |
| Product NDC | 0338-0671 |
| 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; 150; 450 |
| Strength Unit | g/100mL; mg/100mL; mg/100mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
