Product NDC: | 15338-133 |
Proprietary Name: | Klor-Con |
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: | 15338-133 |
Labeler Name: | Apace Packaging LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074726 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000809 |
Package NDC: | 15338-133-30 |
Package Description: | 12 BOTTLE, PLASTIC in 1 CARTON (15338-133-30) > 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
NDC Code | 15338-133-30 |
Proprietary Name | Klor-Con |
Package Description | 12 BOTTLE, PLASTIC in 1 CARTON (15338-133-30) > 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
Product NDC | 15338-133 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Potassium Chloride |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20000809 |
Marketing Category Name | ANDA |
Labeler Name | Apace Packaging LLC |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 20 |
Strength Unit | meq/1 |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |