Product NDC: | 0615-5559 |
Proprietary Name: | Klor Con M |
Non Proprietary Name: | potassium chloride |
Active Ingredient(s): | 10 meq/1 & nbsp; potassium chloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0615-5559 |
Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074726 |
Marketing Category: | ANDA |
Start Marketing Date: | 19981120 |
Package NDC: | 0615-5559-30 |
Package Description: | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-5559-30) > 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Code | 0615-5559-30 |
Proprietary Name | Klor Con M |
Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-5559-30) > 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 0615-5559 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | potassium chloride |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 19981120 |
Marketing Category Name | ANDA |
Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 10 |
Strength Unit | meq/1 |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |