NDC 67046-904

Clorazepate dipotassium

Clorazepate Dipotassium

Clorazepate dipotassium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Clorazepate Dipotassium.

Product ID67046-904_5a409d46-bec0-1e76-e053-2a91aa0ac626
NDC67046-904
Product TypeHuman Prescription Drug
Proprietary NameClorazepate dipotassium
Generic NameClorazepate Dipotassium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-09-28
Marketing CategoryANDA / ANDA
Application NumberANDA076911
Labeler NameContract Pharmacy Services-PA
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 67046-904-60

60 TABLET in 1 BLISTER PACK (67046-904-60)
Marketing Start Date2017-09-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-904-20 [67046090420]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

NDC 67046-904-21 [67046090421]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

NDC 67046-904-30 [67046090430]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

NDC 67046-904-07 [67046090407]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

NDC 67046-904-14 [67046090414]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

NDC 67046-904-60 [67046090460]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

NDC 67046-904-28 [67046090428]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

NDC 67046-904-15 [67046090415]

Clorazepate dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA076911
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CLORAZEPATE DIPOTASSIUM7.5 mg/1

OpenFDA Data

SPL SET ID:5a409d46-bebf-1e76-e053-2a91aa0ac626
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197466
  • 197464
    • UPC Code
  • 0363304553017
  • 0363304554014

    • 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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