| Product NDC: | 55154-6999 |
| Proprietary Name: | POTASSIUM CHLORIDE |
| Non Proprietary Name: | POTASSIUM CHLORIDE |
| Active Ingredient(s): | 149 mg/mL & nbsp; POTASSIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-6999 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080205 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19720316 |
| Package NDC: | 55154-6999-8 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (55154-6999-8) > 10 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 55154-6999-8 |
| Proprietary Name | POTASSIUM CHLORIDE |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (55154-6999-8) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55154-6999 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM CHLORIDE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19720316 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 149 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |