Clonazepam - 68788-9941-3 - (Clonazepam)

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Drug Information of Clonazepam

Product NDC: 68788-9941
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: 68788-9941
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074869
Marketing Category: ANDA
Start Marketing Date: 20120117

Package Information of Clonazepam

Package NDC: 68788-9941-3
Package Description: 30 TABLET in 1 BOTTLE (68788-9941-3)

NDC Information of Clonazepam

NDC Code 68788-9941-3
Proprietary Name Clonazepam
Package Description 30 TABLET in 1 BOTTLE (68788-9941-3)
Product NDC 68788-9941
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120117
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name CLONAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information