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Clorazepate dipotassium - 63304-552-01 - (Clorazepate dipotassium)

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Drug Information of Clorazepate dipotassium

Product NDC: 63304-552
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: 63304-552
Labeler Name: Ranbaxy 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: 63304-552-01
Package Description: 100 TABLET in 1 BOTTLE (63304-552-01)

NDC Information of Clorazepate dipotassium

NDC Code 63304-552-01
Proprietary Name Clorazepate dipotassium
Package Description 100 TABLET in 1 BOTTLE (63304-552-01)
Product NDC 63304-552
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 Ranbaxy Pharmaceuticals 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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