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Klor-Con
Klor-Con - 0245-0035-30 - (Potassium Chloride)
Drug Information of Klor-Con
| Product NDC: | 0245-0035 |
| 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): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Klor-Con
| Product NDC: | 0245-0035 |
| Labeler Name: | Upsher-Smith Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091101 |
Package Information of Klor-Con
| Package NDC: | 0245-0035-30 |
| Package Description: | 30 PACKET in 1 CARTON (0245-0035-30) > 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0035-89) |
NDC Information of Klor-Con
| NDC Code | 0245-0035-30 |
| Proprietary Name | Klor-Con |
| Package Description | 30 PACKET in 1 CARTON (0245-0035-30) > 1 POWDER, FOR SOLUTION in 1 PACKET (0245-0035-89) |
| Product NDC | 0245-0035 |
| 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 | 20 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
