Clonazepam - 21695-260-90 - (Clonazepam)

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Drug Information of Clonazepam

Product NDC: 21695-260
Proprietary Name: Clonazepam
Non Proprietary Name: Clonazepam
Active Ingredient(s): .5    mg/1 & nbsp;   Clonazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clonazepam

Product NDC: 21695-260
Labeler Name: Rebel Distributors
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074569
Marketing Category: ANDA
Start Marketing Date: 20090622

Package Information of Clonazepam

Package NDC: 21695-260-90
Package Description: 90 TABLET in 1 BOTTLE (21695-260-90)

NDC Information of Clonazepam

NDC Code 21695-260-90
Proprietary Name Clonazepam
Package Description 90 TABLET in 1 BOTTLE (21695-260-90)
Product NDC 21695-260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090622
Marketing Category Name ANDA
Labeler Name Rebel Distributors
Substance Name CLONAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information