KLOR-CON is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Sandoz Inc.. The primary component is Potassium Chloride.
| Product ID | 66758-110_83a1d758-b0ce-41e6-8ac2-d0fcca999221 | 
| NDC | 66758-110 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | KLOR-CON | 
| Generic Name | Potassium Chloride | 
| Dosage Form | Tablet, Film Coated, Extended Release | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2014-09-01 | 
| Marketing Category | NDA / NDA | 
| Application Number | NDA019123 | 
| Labeler Name | Sandoz Inc. | 
| Substance Name | POTASSIUM CHLORIDE | 
| Active Ingredient Strength | 600 mg/1 | 
| Pharm Classes | Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2020-12-31 | 
| Marketing Start Date | 2014-09-01 | 
| Marketing End Date | 2021-09-30 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | NDA | 
| Application Number | NDA019123 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2014-09-01 | 
| Marketing Category | NDA | 
| Application Number | NDA019123 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2014-09-01 | 
| Marketing End Date | 2017-12-31 | 
| Marketing Category | NDA | 
| Application Number | NDA019123 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2014-09-01 | 
| Marketing Category | NDA | 
| Application Number | NDA019123 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2014-09-01 | 
| Marketing End Date | 2017-12-31 | 
| Marketing Category | NDA | 
| Application Number | NDA019123 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2014-09-01 | 
| Marketing Category | NDA | 
| Application Number | NDA019123 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2014-09-01 | 
| Ingredient | Strength | 
|---|---|
| POTASSIUM CHLORIDE | 600 mg/1 | 
| SPL SET ID: | 466170e9-e158-4ccd-b7a3-53dc8c3cd749 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0440-8110 | Klor-Con | Klor-Con | 
| 0615-8045 | KLOR-CON | KLOR-CON | 
| 43353-064 | KLOR-CON | KLOR-CON | 
| 0245-0041 | Klor-Con | Klor-Con | 
| 0245-0040 | Klor-Con | Klor-Con | 
| 0245-0360 | KLOR-CON | KLOR-CON | 
| 55154-0927 | KLOR-CON | KLOR-CON | 
| 55289-697 | Klor-Con | Klor-Con | 
| 65084-464 | KLOR-CON | KLOR-CON | 
| 65084-465 | KLOR-CON | KLOR-CON | 
| 66758-160 | KLOR-CON | KLOR-CON | 
| 66758-110 | KLOR-CON | KLOR-CON | 
| 67544-237 | Klor-Con | Klor-Con | 
| 67544-154 | Klor-Con | Klor-Con | 
| 0245-5315 | KLOR-CON | KLOR-CON | 
| 0245-5316 | KLOR-CON | KLOR-CON | 
| 0074-3023 | K-Tab | Potassium Chloride | 
| 0074-3058 | K-Tab | Potassium Chloride | 
| 0074-3278 | K-Tab | Potassium Chloride | 
| 0074-7804 | K-Tab | Potassium Chloride | 
| 0220-2891 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0220-2951 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0220-2952 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0220-2953 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0220-2954 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0220-2955 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0220-2956 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0220-2957 | Kali muriaticum | POTASSIUM CHLORIDE | 
| 0121-0841 | Potassium Chloride | POTASSIUM CHLORIDE | 
| 0121-1680 | Potassium Chloride | POTASSIUM CHLORIDE | 
| 0121-2520 | Potassium Chloride | POTASSIUM CHLORIDE | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  KLOR-CON  73592767  1415559 Live/Registered | UPSHER-SMITH LABORATORIES, INC. 1986-04-11 | 
|  KLOR-CON  73173477  1112591 Dead/Cancelled | UPSHER-SMITH LABORATORIES, INC. 1978-08-04 |