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Clorazepate Dipotassium - 54868-2133-2 - (clorazepate dipotassium)

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Drug Information of Clorazepate Dipotassium

Product NDC: 54868-2133
Proprietary Name: Clorazepate Dipotassium
Non Proprietary Name: clorazepate dipotassium
Active Ingredient(s): 3.75    mg/1 & nbsp;   clorazepate dipotassium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clorazepate Dipotassium

Product NDC: 54868-2133
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071858
Marketing Category: ANDA
Start Marketing Date: 19960524

Package Information of Clorazepate Dipotassium

Package NDC: 54868-2133-2
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-2133-2)

NDC Information of Clorazepate Dipotassium

NDC Code 54868-2133-2
Proprietary Name Clorazepate Dipotassium
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-2133-2)
Product NDC 54868-2133
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clorazepate dipotassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960524
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CLORAZEPATE DIPOTASSIUM
Strength Number 3.75
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clorazepate Dipotassium


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