| Product NDC: | 15338-122 |
| Proprietary Name: | Klor-Con |
| 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: | 15338-122 |
| Labeler Name: | Apace Packaging LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074726 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000809 |
| Package NDC: | 15338-122-30 |
| Package Description: | 12 BOTTLE, PLASTIC in 1 CARTON (15338-122-30) > 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
| NDC Code | 15338-122-30 |
| Proprietary Name | Klor-Con |
| Package Description | 12 BOTTLE, PLASTIC in 1 CARTON (15338-122-30) > 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
| Product NDC | 15338-122 |
| 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 | 10 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |