Clonazepam - 66336-588-30 - (clonazepam)

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Drug Information of Clonazepam

Product NDC: 66336-588
Proprietary Name: Clonazepam
Non Proprietary Name: clonazepam
Active Ingredient(s): 1    mg/1 & nbsp;   clonazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clonazepam

Product NDC: 66336-588
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077856
Marketing Category: ANDA
Start Marketing Date: 20060628

Package Information of Clonazepam

Package NDC: 66336-588-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (66336-588-30)

NDC Information of Clonazepam

NDC Code 66336-588-30
Proprietary Name Clonazepam
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (66336-588-30)
Product NDC 66336-588
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clonazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060628
Marketing Category Name ANDA
Labeler Name Dispensing Solutions, Inc.
Substance Name CLONAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information