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Clorazepate Dipotassium - 43063-030-06 - (clorazepate dipotassium)

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Drug Information of Clorazepate Dipotassium

Product NDC: 43063-030
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: 43063-030
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071858
Marketing Category: ANDA
Start Marketing Date: 20100729

Package Information of Clorazepate Dipotassium

Package NDC: 43063-030-06
Package Description: 6 TABLET in 1 BOTTLE, PLASTIC (43063-030-06)

NDC Information of Clorazepate Dipotassium

NDC Code 43063-030-06
Proprietary Name Clorazepate Dipotassium
Package Description 6 TABLET in 1 BOTTLE, PLASTIC (43063-030-06)
Product NDC 43063-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clorazepate dipotassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100729
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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