NDC 63629-2703

Potassium Chloride

Potassium Chloride

Potassium Chloride is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Potassium Chloride.

Product ID63629-2703_1acc65d7-89af-41e5-800c-fe63b15f94c8
NDC63629-2703
Product TypeHuman Prescription Drug
Proprietary NamePotassium Chloride
Generic NamePotassium Chloride
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2004-08-18
Marketing CategoryANDA / ANDA
Application NumberANDA076368
Labeler NameBryant Ranch Prepack
Substance NamePOTASSIUM CHLORIDE
Active Ingredient Strength20 meq/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 63629-2703-1

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-1)
Marketing Start Date2007-12-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-2703-3 [63629270303]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076368
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-12-24
Inactivation Date2020-01-31
Reactivation Date2020-02-25

NDC 63629-2703-6 [63629270306]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076368
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-01-12
Inactivation Date2020-01-31
Reactivation Date2020-02-25

NDC 63629-2703-5 [63629270305]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076368
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-01-12
Inactivation Date2020-01-31
Reactivation Date2020-02-25

NDC 63629-2703-1 [63629270301]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076368
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-12-24
Inactivation Date2020-01-31
Reactivation Date2020-02-25

NDC 63629-2703-2 [63629270302]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076368
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-12-24
Inactivation Date2020-01-31
Reactivation Date2020-02-25

NDC 63629-2703-4 [63629270304]

Potassium Chloride TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076368
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-12-24
Inactivation Date2020-01-31
Reactivation Date2020-02-25

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM CHLORIDE20 meq/1

OpenFDA Data

SPL SET ID:6766515e-12f9-4c45-977c-e099c74fe931
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1801294
  • 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 "Potassium Chloride" or generic name "Potassium Chloride"

    NDCBrand NameGeneric Name
    0121-0841Potassium ChloridePOTASSIUM CHLORIDE
    0121-1680Potassium ChloridePOTASSIUM CHLORIDE
    0121-2520Potassium ChloridePOTASSIUM CHLORIDE
    68001-235Potassium ChloridePotassium Chloride
    68001-259Potassium ChloridePotassium Chloride
    68001-303Potassium ChloridePotassium Chloride
    68001-367potassium chloridepotassium chloride
    0409-7074Potassium ChloridePotassium Chloride
    0409-6651POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
    0409-7075Potassium ChloridePotassium Chloride
    0409-6653POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
    0409-6635POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
    0409-7077Potassium ChloridePotassium Chloride
    0409-7076Potassium ChloridePotassium Chloride
    68071-1933Potassium ChloridePotassium Chloride
    68071-3153Potassium ChloridePotassium Chloride
    68071-3274Potassium ChloridePotassium Chloride
    68071-4078Potassium ChloridePotassium Chloride
    68071-4296Potassium ChloridePotassium Chloride
    68071-4708Potassium ChloridePotassium Chloride
    68071-4716potassium chloridepotassium chloride
    68084-419potassium chloridepotassium chloride
    68084-524Potassium ChloridePotassium Chloride
    68084-632Potassium ChloridePotassium Chloride
    68084-360Potassium ChloridePotassium Chloride
    68151-0609Potassium ChloridePotassium Chloride
    68180-799Potassium ChloridePotassium Chloride
    68180-798Potassium ChloridePotassium Chloride
    68382-701POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
    68382-398Potassium ChloridePotassium Chloride
    68382-702POTASSIUM CHLORIDEPOTASSIUM CHLORIDE
    68382-320Potassium ChloridePotassium Chloride
    68382-600Potassium ChloridePotassium Chloride
    68382-776Potassium ChloridePotassium Chloride
    68462-357Potassium ChloridePotassium Chloride
    68462-472potassium chloridepotassium chloride
    68462-471potassium chloridepotassium chloride
    68788-6771Potassium ChloridePotassium Chloride
    68788-6772Potassium ChloridePotassium Chloride
    69238-1458Potassium ChloridePotassium Chloride
    69238-1459Potassium ChloridePotassium Chloride
    0574-0181Potassium ChloridePotassium Chloride
    0574-0180Potassium ChloridePotassium Chloride
    70436-001Potassium ChloridePotassium Chloride
    70518-0057Potassium ChloridePotassium Chloride
    70518-0152Potassium ChloridePotassium Chloride
    70518-0348Potassium ChloridePotassium Chloride
    70436-002Potassium ChloridePotassium Chloride
    70518-1068Potassium ChloridePotassium Chloride
    70518-1203Potassium ChloridePotassium Chloride

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