Clonazepam - 51079-882-21 - (clonazepam)

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Drug Information of Clonazepam

Product NDC: 51079-882
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: 51079-882
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075150
Marketing Category: ANDA
Start Marketing Date: 20110708

Package Information of Clonazepam

Package NDC: 51079-882-21
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (51079-882-21)

NDC Information of Clonazepam

NDC Code 51079-882-21
Proprietary Name Clonazepam
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (51079-882-21)
Product NDC 51079-882
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clonazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110708
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name CLONAZEPAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information