NDC 63629-3859

Clorazepate Dipotassium

Clorazepate Dipotassium

Clorazepate Dipotassium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Clorazepate Dipotassium.

Product ID63629-3859_d42b3b3a-fe63-40d9-acc1-90a515a03969
NDC63629-3859
Product TypeHuman Prescription Drug
Proprietary NameClorazepate Dipotassium
Generic NameClorazepate Dipotassium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2000-04-27
Marketing CategoryANDA / ANDA
Application NumberANDA075731
Labeler NameBryant Ranch Prepack
Substance NameCLORAZEPATE DIPOTASSIUM
Active Ingredient Strength15 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63629-3859-1

30 TABLET in 1 BOTTLE (63629-3859-1)
Marketing Start Date2000-04-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-3859-1 [63629385901]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA075731
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-10-28
Marketing End Date2010-09-01

NDC 63629-3859-3 [63629385903]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA075731
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-10-28
Marketing End Date2010-09-01

NDC 63629-3859-2 [63629385902]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA075731
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-10-28
Marketing End Date2010-09-01

NDC 63629-3859-4 [63629385904]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA075731
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-10-28
Marketing End Date2010-09-01

Drug Details

Active Ingredients

IngredientStrength
CLORAZEPATE DIPOTASSIUM15 mg/1

OpenFDA Data

SPL SET ID:5a82b479-64bd-474f-93e2-c97ce5cce9df
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197464

    • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

    NDC Crossover Matching brand name "Clorazepate Dipotassium" or generic name "Clorazepate Dipotassium"

    NDCBrand NameGeneric Name
    0378-0030Clorazepate Dipotassiumclorazepate dipotassium
    0378-0040Clorazepate Dipotassiumclorazepate dipotassium
    0378-0070Clorazepate Dipotassiumclorazepate dipotassium
    13107-319CLORAZEPATE DIPOTASSIUMCLORAZEPATE DIPOTASSIUM
    13107-320CLORAZEPATE DIPOTASSIUMCLORAZEPATE DIPOTASSIUM
    13107-321CLORAZEPATE DIPOTASSIUMCLORAZEPATE DIPOTASSIUM
    21695-433Clorazepate DipotassiumClorazepate Dipotassium
    21695-434Clorazepate DipotassiumClorazepate Dipotassium
    43063-030Clorazepate Dipotassiumclorazepate dipotassium
    43063-164Clorazepate Dipotassiumclorazepate dipotassium
    43063-350Clorazepate Dipotassiumclorazepate dipotassium
    43063-893Clorazepate DipotassiumClorazepate Dipotassium
    51672-4042Clorazepate DipotassiumClorazepate Dipotassium
    51672-4043Clorazepate DipotassiumClorazepate Dipotassium
    51672-4044Clorazepate DipotassiumClorazepate Dipotassium
    60505-4754Clorazepate DipotassiumClorazepate Dipotassium
    63304-552Clorazepate dipotassiumClorazepate dipotassium
    63304-553Clorazepate dipotassiumClorazepate dipotassium
    63304-554Clorazepate dipotassiumClorazepate dipotassium
    63629-3646Clorazepate DipotassiumClorazepate Dipotassium
    63629-3858Clorazepate dipotassiumClorazepate dipotassium
    63629-3859Clorazepate DipotassiumClorazepate Dipotassium
    67046-906Clorazepate DipotassiumClorazepate Dipotassium
    67046-907Clorazepate dipotassiumClorazepate dipotassium
    67046-904Clorazepate dipotassiumClorazepate dipotassium
    55292-304Tranxeneclorazepate dipotassium
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