| NDC Code | 0245-5315-11 | 
|---|
			| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-11) | 
|---|
			| Product NDC | 0245-5315 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Klor-con | 
|---|
			
			| Non-Proprietary Name | Potassium Chloride | 
|---|
			| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 19860417 | 
|---|
			
			| Marketing Category Name | NDA | 
|---|
			| Application Number | NDA019123 | 
|---|
			| Manufacturer | Upsher-Smith Laboratories, LLC | 
|---|
			| Substance Name | POTASSIUM CHLORIDE | 
|---|
			| Strength | 600 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] | 
|---|