Product NDC: | 55154-1478 |
Proprietary Name: | Potassium Chloride |
Non Proprietary Name: | Potassium Chloride |
Active Ingredient(s): | 20 meq/1 & nbsp; Potassium Chloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-1478 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074726 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090810 |
Package NDC: | 55154-1478-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-1478-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Code | 55154-1478-0 |
Proprietary Name | Potassium Chloride |
Package Description | 10 BLISTER PACK in 1 BAG (55154-1478-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 55154-1478 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Potassium Chloride |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20090810 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 20 |
Strength Unit | meq/1 |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |