Clonazepam - 35356-719-01 - (Clonazepam)

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Drug Information of Clonazepam

Product NDC: 35356-719
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: 35356-719
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074869
Marketing Category: ANDA
Start Marketing Date: 20090213

Package Information of Clonazepam

Package NDC: 35356-719-01
Package Description: 120 TABLET in 1 BOTTLE (35356-719-01)

NDC Information of Clonazepam

NDC Code 35356-719-01
Proprietary Name Clonazepam
Package Description 120 TABLET in 1 BOTTLE (35356-719-01)
Product NDC 35356-719
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 Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name CLONAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information