Product NDC: | 0245-0037 |
Proprietary Name: | Klor-Con |
Non Proprietary Name: | Potassium Chloride |
Active Ingredient(s): | 25 meq/1 & nbsp; Potassium Chloride |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0245-0037 |
Labeler Name: | Upsher-Smith Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20091101 |
Package NDC: | 0245-0037-01 |
Package Description: | 100 PACKET in 1 CARTON (0245-0037-01) > 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0037-89) |
NDC Code | 0245-0037-01 |
Proprietary Name | Klor-Con |
Package Description | 100 PACKET in 1 CARTON (0245-0037-01) > 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0037-89) |
Product NDC | 0245-0037 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Potassium Chloride |
Dosage Form Name | POWDER, FOR SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20091101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Upsher-Smith Laboratories, Inc. |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 25 |
Strength Unit | meq/1 |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |