NDC 43063-030

Clorazepate Dipotassium

Clorazepate Dipotassium

Clorazepate Dipotassium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pd-rx Pharmaceuticals, Inc.. The primary component is Clorazepate Dipotassium.

Product ID43063-030_816566bf-b8a1-606f-e053-2a91aa0ab8c9
NDC43063-030
Product TypeHuman Prescription Drug
Proprietary NameClorazepate Dipotassium
Generic NameClorazepate Dipotassium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1987-07-17
Marketing CategoryANDA / ANDA
Application NumberANDA071858
Labeler NamePD-Rx Pharmaceuticals, Inc.
Substance NameCLORAZEPATE DIPOTASSIUM
Active Ingredient Strength15 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43063-030-03

3 TABLET in 1 BOTTLE, PLASTIC (43063-030-03)
Marketing Start Date2010-06-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43063-030-10 [43063003010]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA071858
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-17

NDC 43063-030-06 [43063003006]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA071858
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-17

NDC 43063-030-12 [43063003012]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA071858
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-17

NDC 43063-030-03 [43063003003]

Clorazepate Dipotassium TABLET
Marketing CategoryANDA
Application NumberANDA071858
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-06-17

Drug Details

Active Ingredients

IngredientStrength
CLORAZEPATE DIPOTASSIUM15 mg/1

OpenFDA Data

SPL SET ID:54722d55-d620-488f-87eb-e1e3b129c2f9
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
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.