| Product NDC: | 42806-098 | 
| Proprietary Name: | EPIKLOR | 
| Non Proprietary Name: | Potassium Chloride | 
| Active Ingredient(s): | 1.5 g/1.77g & nbsp; Potassium Chloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | POWDER, FOR SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 42806-098 | 
| Labeler Name: | Epic Pharma, LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20100201 | 
| Package NDC: | 42806-098-30 | 
| Package Description: | 30 PACKET in 1 CARTON (42806-098-30) > 1.77 g in 1 PACKET | 
| NDC Code | 42806-098-30 | 
| Proprietary Name | EPIKLOR | 
| Package Description | 30 PACKET in 1 CARTON (42806-098-30) > 1.77 g in 1 PACKET | 
| Product NDC | 42806-098 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Potassium Chloride | 
| Dosage Form Name | POWDER, FOR SOLUTION | 
| Route Name | ORAL | 
| Start Marketing Date | 20100201 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Epic Pharma, LLC | 
| Substance Name | POTASSIUM CHLORIDE | 
| Strength Number | 1.5 | 
| Strength Unit | g/1.77g | 
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |