Clonazepam - 52959-761-10 - (Clonazepam)

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Drug Information of Clonazepam

Product NDC: 52959-761
Proprietary Name: Clonazepam
Non Proprietary Name: Clonazepam
Active Ingredient(s): 2    mg/1 & nbsp;   Clonazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clonazepam

Product NDC: 52959-761
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074869
Marketing Category: ANDA
Start Marketing Date: 20090213

Package Information of Clonazepam

Package NDC: 52959-761-10
Package Description: 10 TABLET in 1 BOTTLE (52959-761-10)

NDC Information of Clonazepam

NDC Code 52959-761-10
Proprietary Name Clonazepam
Package Description 10 TABLET in 1 BOTTLE (52959-761-10)
Product NDC 52959-761
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090213
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name CLONAZEPAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information