NDC 0074-3058

K-Tab

Potassium Chloride

K-Tab is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Abbvie Inc.. The primary component is Potassium Chloride.

Product ID0074-3058_269b29d0-1d90-1622-ef7d-d54f7bd47409
NDC0074-3058
Product TypeHuman Prescription Drug
Proprietary NameK-Tab
Generic NamePotassium Chloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date1980-06-09
Marketing CategoryNDA / NDA
Application NumberNDA018279
Labeler NameAbbVie Inc.
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 0074-3058-41

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-3058-41)
Marketing Start Date1980-06-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0074-3058-30 [00074305830]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-09-30
Marketing End Date2017-07-10

NDC 0074-3058-41 [00074305841]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1980-06-09

NDC 0074-3058-90 [00074305890]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-09-30
Marketing End Date2017-07-10

NDC 0074-3058-46 [00074305846]

K-Tab TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA018279
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1980-06-09

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM CHLORIDE600 mg/1

OpenFDA Data

SPL SET ID:6594df99-d8ce-49b9-3fbe-9ec7cdc9199b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312529
  • 1541594
  • 628953
  • 198116
  • 670031
  • 1483340
  • UPC Code
  • 0300743023138
  • 0300743278132
  • 0300743058413
  • 0300747804191
  • 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]
    • 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 "K-Tab" or generic name "Potassium Chloride"

    NDCBrand NameGeneric Name
    0074-3023K-TabPotassium Chloride
    0074-3058K-TabPotassium Chloride
    0074-3278K-TabPotassium Chloride
    0074-7804K-TabPotassium Chloride
    70518-0220K-TabK-Tab
    43353-790K-TabK-Tab
    53808-0277K-TABK-TAB
    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 [K-Tab]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    K-TAB
    K-TAB
    86020923 4491093 Live/Registered
    AbbVie Inc.
    2013-07-26
    K-TAB
    K-TAB
    74297051 1814878 Dead/Cancelled
    SCOTT OFFICE SYSTEMS, LLC
    1992-07-21
    K-TAB
    K-TAB
    73226881 1266633 Dead/Cancelled
    Abbott Laboratories
    1979-08-09

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