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Clorazepate dipotassium - 43063-382-10 - (Clorazepate dipotassium)

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Drug Information of Clorazepate dipotassium

Product NDC: 43063-382
Proprietary Name: Clorazepate dipotassium
Non Proprietary Name: Clorazepate dipotassium
Active Ingredient(s): 15    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: 43063-382
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076911
Marketing Category: ANDA
Start Marketing Date: 20050114

Package Information of Clorazepate dipotassium

Package NDC: 43063-382-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (43063-382-10)

NDC Information of Clorazepate dipotassium

NDC Code 43063-382-10
Proprietary Name Clorazepate dipotassium
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (43063-382-10)
Product NDC 43063-382
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clorazepate dipotassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050114
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name CLORAZEPATE DIPOTASSIUM
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clorazepate dipotassium


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