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] |