NDC 0245-5315

KLOR-CON

Potassium Chloride

KLOR-CON is a Oral Tablet, Film Coated, 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 ID0245-5315_0907ea1c-82f3-4ba8-9d1b-3f4fa104d7a2
NDC0245-5315
Product TypeHuman Prescription Drug
Proprietary NameKLOR-CON
Generic NamePotassium Chloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date1986-04-17
Marketing CategoryNDA / NDA
Application NumberNDA019123
Labeler NameUpsher-Smith Laboratories, LLC
Substance NamePOTASSIUM CHLORIDE
Active Ingredient Strength600 mg/1
Pharm ClassesPotassium 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 FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0245-5315-01

100 BLISTER PACK in 1 BLISTER PACK (0245-5315-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0245-5315-89)
Marketing Start Date2019-06-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0245-5315-89 [00245531589]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1986-04-17

NDC 0245-5315-11 [00245531511]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-21

NDC 0245-5315-01 [00245531501]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-21

NDC 0245-5315-15 [00245531515]

KLOR-CON TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA019123
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-06-21

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM CHLORIDE600 mg/1

OpenFDA Data

SPL SET ID:1ff53330-065c-4213-9c0c-ac498621d09d
Manufacturer
UNII
UPC Code
  • 0302455316119
  • 0302455315112
  • Pharmacological Class

    • 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 Crossover Matching brand name "KLOR-CON" or generic name "Potassium Chloride"

    NDCBrand NameGeneric Name
    0440-8110Klor-ConKlor-Con
    0615-8045KLOR-CONKLOR-CON
    43353-064KLOR-CONKLOR-CON
    0245-0041Klor-ConKlor-Con
    0245-0040Klor-ConKlor-Con
    0245-0360KLOR-CONKLOR-CON
    55154-0927KLOR-CONKLOR-CON
    55289-697Klor-ConKlor-Con
    65084-464KLOR-CONKLOR-CON
    65084-465KLOR-CONKLOR-CON
    66758-160KLOR-CONKLOR-CON
    66758-110KLOR-CONKLOR-CON
    67544-237Klor-ConKlor-Con
    67544-154Klor-ConKlor-Con
    0245-5315KLOR-CONKLOR-CON
    0245-5316KLOR-CONKLOR-CON
    0074-3023K-TabPotassium Chloride
    0074-3058K-TabPotassium Chloride
    0074-3278K-TabPotassium Chloride
    0074-7804K-TabPotassium Chloride
    0220-2891Kali muriaticumPOTASSIUM CHLORIDE
    0220-2951Kali muriaticumPOTASSIUM CHLORIDE
    0220-2952Kali muriaticumPOTASSIUM CHLORIDE
    0220-2953Kali muriaticumPOTASSIUM CHLORIDE
    0220-2954Kali muriaticumPOTASSIUM CHLORIDE
    0220-2955Kali muriaticumPOTASSIUM CHLORIDE
    0220-2956Kali muriaticumPOTASSIUM CHLORIDE
    0220-2957Kali muriaticumPOTASSIUM CHLORIDE
    0121-0841Potassium ChloridePOTASSIUM CHLORIDE
    0121-1680Potassium ChloridePOTASSIUM CHLORIDE
    0121-2520Potassium ChloridePOTASSIUM CHLORIDE

    Trademark Results [KLOR-CON]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    KLOR-CON
    KLOR-CON
    73592767 1415559 Live/Registered
    UPSHER-SMITH LABORATORIES, INC.
    1986-04-11
    KLOR-CON
    KLOR-CON
    73173477 1112591 Dead/Cancelled
    UPSHER-SMITH LABORATORIES, INC.
    1978-08-04

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.