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Potassium Chloride
Potassium Chloride - 0603-1534-58 - (potassium chloride)
Drug Information of Potassium Chloride
| Product NDC: | 0603-1534 |
| Proprietary Name: | Potassium Chloride |
| Non Proprietary Name: | potassium chloride |
| Active Ingredient(s): | 20 meq/15mL & nbsp; potassium chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Chloride
| Product NDC: | 0603-1534 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19960801 |
Package Information of Potassium Chloride
| Package NDC: | 0603-1534-58 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0603-1534-58) |
NDC Information of Potassium Chloride
| NDC Code | 0603-1534-58 |
| Proprietary Name | Potassium Chloride |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0603-1534-58) |
| Product NDC | 0603-1534 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | potassium chloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19960801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 20 |
| Strength Unit | meq/15mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
