Clonazepam - 0093-0832-19 - (Clonazepam)

Alphabetical Index


Drug Information of Clonazepam

Product NDC: 0093-0832
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: 0093-0832
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074569
Marketing Category: ANDA
Start Marketing Date: 19960918

Package Information of Clonazepam

Package NDC: 0093-0832-19
Package Description: 1 TABLET in 1 BLISTER PACK (0093-0832-19)

NDC Information of Clonazepam

NDC Code 0093-0832-19
Proprietary Name Clonazepam
Package Description 1 TABLET in 1 BLISTER PACK (0093-0832-19)
Product NDC 0093-0832
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960918
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CLONAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information