NDC 68382-537

Potassium Citrate

Potassium Citrate

Potassium Citrate is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Zydus Pharmaceuticals (usa) Inc.. The primary component is Potassium Citrate.

Product ID68382-537_60e001b8-de37-485c-b258-b7c06fba2ddd
NDC68382-537
Product TypeHuman Prescription Drug
Proprietary NamePotassium Citrate
Generic NamePotassium Citrate
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2014-08-12
Marketing CategoryANDA / ANDA
Application NumberANDA203546
Labeler NameZydus Pharmaceuticals (USA) Inc.
Substance NamePOTASSIUM CITRATE
Active Ingredient Strength10 meq/1
Pharm ClassesAcidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68382-537-01

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-01)
Marketing Start Date2014-08-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68382-537-06 [68382053706]

Potassium Citrate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203546
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-12

NDC 68382-537-05 [68382053705]

Potassium Citrate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203546
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-12

NDC 68382-537-01 [68382053701]

Potassium Citrate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203546
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-08-12

NDC 68382-537-10 [68382053710]

Potassium Citrate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203546
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-12

NDC 68382-537-16 [68382053716]

Potassium Citrate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203546
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-12

NDC 68382-537-30 [68382053730]

Potassium Citrate TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA203546
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-08-12

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM CITRATE10 meq/1

OpenFDA Data

SPL SET ID:1a839f91-9bbd-4f46-b350-c5e8074b5db7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 199381
  • 898490
  • 199376
    • UPC Code
  • 0368382536013

    • Pharmacological Class

    • Acidifying Activity [MoA]
    • Calculi Dissolution Agent [EPC]
    • Anti-coagulant [EPC]
    • Decreased Coagulation Factor Activity [PE]
    • Calcium Chelating Activity [MoA]

    Medicade Reported Pricing

    68382053701 POTASSIUM CITRATE ER 10 MEQ TB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Potassium Citrate" or generic name "Potassium Citrate"

    NDCBrand NameGeneric Name
    0245-0070Potassium Citratepotassium citrate
    0245-0071Potassium Citratepotassium citrate
    68084-850Potassium CitratePotassium Citrate
    68382-538Potassium CitratePotassium Citrate
    68382-536Potassium CitratePotassium Citrate
    68382-537Potassium CitratePotassium Citrate
    0591-2742Potassium CitratePotassium Citrate
    0591-2682Potassium CitratePotassium Citrate
    0591-2729Potassium CitratePotassium Citrate
    44523-415Potassium CitratePotassium Citrate
    65841-536Potassium CitratePotassium Citrate
    65841-537Potassium CitratePotassium Citrate
    65841-538Potassium CitratePotassium Citrate
    63629-7980Potassium CitratePotassium Citrate
    62559-292Potassium CitratePotassium Citrate
    62559-291Potassium CitratePotassium Citrate
    42291-500Potassium CitratePotassium Citrate
    63629-1966Potassium CitratePotassium Citrate
    69452-193Potassium CitratePotassium Citrate
    42291-499Potassium CitratePotassium Citrate
    63629-1967Potassium CitratePotassium Citrate
    69452-194Potassium CitratePotassium Citrate
    0178-0600UROCIT-Kpotassium citrate
    0178-0610UROCIT-Kpotassium citrate
    0178-0615UROCIT-Kpotassium citrate
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