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Potassium Chloride
Potassium Chloride - 0338-0705-41 - (POTASSIUM CHLORIDE)
Drug Information of Potassium Chloride
| Product NDC: | 0338-0705 |
| Proprietary Name: | Potassium Chloride |
| Non Proprietary Name: | POTASSIUM CHLORIDE |
| Active Ingredient(s): | 200 meq/1000mL & nbsp; POTASSIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Chloride
| Product NDC: | 0338-0705 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019904 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19891226 |
Package Information of Potassium Chloride
| Package NDC: | 0338-0705-41 |
| Package Description: | 24 BAG in 1 CARTON (0338-0705-41) > 50 mL in 1 BAG |
NDC Information of Potassium Chloride
| NDC Code | 0338-0705-41 |
| Proprietary Name | Potassium Chloride |
| Package Description | 24 BAG in 1 CARTON (0338-0705-41) > 50 mL in 1 BAG |
| Product NDC | 0338-0705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19891226 |
| Marketing Category Name | NDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 200 |
| Strength Unit | meq/1000mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
