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Clorazepate Dipotassium - 21695-434-60 - (Clorazepate Dipotassium)

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Drug Information of Clorazepate Dipotassium

Product NDC: 21695-434
Proprietary Name: Clorazepate Dipotassium
Non Proprietary Name: Clorazepate Dipotassium
Active Ingredient(s): 7.5    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: 21695-434
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075731
Marketing Category: ANDA
Start Marketing Date: 20000427

Package Information of Clorazepate Dipotassium

Package NDC: 21695-434-60
Package Description: 60 TABLET in 1 BOTTLE (21695-434-60)

NDC Information of Clorazepate Dipotassium

NDC Code 21695-434-60
Proprietary Name Clorazepate Dipotassium
Package Description 60 TABLET in 1 BOTTLE (21695-434-60)
Product NDC 21695-434
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clorazepate Dipotassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000427
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CLORAZEPATE DIPOTASSIUM
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clorazepate Dipotassium


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