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Potassium Chloride in Sodium Chloride
Potassium Chloride in Sodium Chloride - 0338-0704-34 - (Potassium Chloride and Sodium Chloride)
Drug Information of Potassium Chloride in Sodium Chloride
| Product NDC: | 0338-0704 |
| Proprietary Name: | Potassium Chloride in Sodium Chloride |
| Non Proprietary Name: | Potassium Chloride and Sodium Chloride |
| Active Ingredient(s): | 150; 450 mg/100mL; mg/100mL & nbsp; Potassium Chloride and Sodium Chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Chloride in Sodium Chloride
| Product NDC: | 0338-0704 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017648 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19790202 |
Package Information of Potassium Chloride in Sodium Chloride
| Package NDC: | 0338-0704-34 |
| Package Description: | 1000 mL in 1 BAG (0338-0704-34) |
NDC Information of Potassium Chloride in Sodium Chloride
| NDC Code | 0338-0704-34 |
| Proprietary Name | Potassium Chloride in Sodium Chloride |
| Package Description | 1000 mL in 1 BAG (0338-0704-34) |
| Product NDC | 0338-0704 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Chloride 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 | POTASSIUM CHLORIDE; SODIUM CHLORIDE |
| Strength Number | 150; 450 |
| Strength Unit | mg/100mL; mg/100mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
