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] |