NDC 63304-553

Clorazepate dipotassium

Clorazepate Dipotassium

Clorazepate dipotassium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ranbaxy Pharmaceuticals Inc.. The primary component is Clorazepate Dipotassium.

Product ID63304-553_9288b398-2811-4f9b-a088-c719de4dc8f4
NDC63304-553
Product TypeHuman Prescription Drug
Proprietary NameClorazepate dipotassium
Generic NameClorazepate Dipotassium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2005-01-14
Marketing CategoryANDA / ANDA
Application NumberANDA076911
Labeler NameRanbaxy Pharmaceuticals Inc.
Substance NameCLORAZEPATE DIPOTASSIUM
Active Ingredient Strength8 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 63304-553-01

100 TABLET in 1 BOTTLE (63304-553-01)
Marketing Start Date2005-01-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63304-553-01 [63304055301]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-01-14
Inactivation Date2020-01-31

NDC 63304-553-10 [63304055310]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-01-14
Inactivation Date2020-01-31

NDC 63304-553-05 [63304055305]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-01-14
Inactivation Date2020-01-31

NDC 63304-553-30 [63304055330]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-01-14
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CLORAZEPATE DIPOTASSIUM7.5 mg/1

OpenFDA Data

SPL SET ID:6e9edbfc-1950-4893-9d38-e82b119ddb9a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197466
  • 197465
  • 197464
  • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

    Medicade Reported Pricing

    63304055305 CLORAZEPATE 7.5 MG TABLET

    Pricing Unit: EA | Drug Type:

    63304055301 CLORAZEPATE 7.5 MG TABLET

    Pricing Unit: EA | Drug Type:

    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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