Klor-Con Sprinkle is a Oral Capsule, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Upsher-smith Laboratories, Llc. The primary component is Potassium Chloride.
| Product ID | 0245-0102_0f47c0ea-170c-457a-b2c0-9f49f435ad7b |
| NDC | 0245-0102 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Klor-Con Sprinkle |
| Generic Name | Potassium Chloride |
| Dosage Form | Capsule, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-07-10 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA203106 |
| Labeler Name | Upsher-Smith Laboratories, LLC |
| Substance Name | POTASSIUM CHLORIDE |
| Active Ingredient Strength | 750 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 | 2021-12-31 |
| Marketing Start Date | 2015-07-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA203106 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-10 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA203106 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-10 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA203106 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-10 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA203106 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-10 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA203106 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-10 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA203106 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-07-10 |
| Marketing End Date | 2015-12-31 |
| Ingredient | Strength |
|---|---|
| POTASSIUM CHLORIDE | 750 mg/1 |
| SPL SET ID: | c630324c-0f67-4276-8328-16fbe1db2e89 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0615-8066 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 0615-8085 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 0245-0101 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 0245-5320 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 0245-5321 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 0245-0102 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 66758-205 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 66758-202 | Klor-Con Sprinkle | Klor-Con Sprinkle |
| 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 |