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Klor-Con
Klor-Con - 68645-201-54 - (Potassium Chloride)
Drug Information of Klor-Con
| Product NDC: | 68645-201 |
| Proprietary Name: | Klor-Con |
| Non Proprietary Name: | Potassium Chloride |
| Active Ingredient(s): | 600 mg/1 & nbsp; Potassium Chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Klor-Con
| Product NDC: | 68645-201 |
| Labeler Name: | Legacy Pharmaceutical Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019123 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19860417 |
Package Information of Klor-Con
| Package NDC: | 68645-201-54 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-201-54) |
NDC Information of Klor-Con
| NDC Code | 68645-201-54 |
| Proprietary Name | Klor-Con |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-201-54) |
| Product NDC | 68645-201 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Chloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19860417 |
| Marketing Category Name | NDA |
| Labeler Name | Legacy Pharmaceutical Packaging |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
