Clonazepam - 49349-031-02 - (Clonazepan)

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Drug Information of Clonazepam

Product NDC: 49349-031
Proprietary Name: Clonazepam
Non Proprietary Name: Clonazepan
Active Ingredient(s): .5    mg/1 & nbsp;   Clonazepan
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clonazepam

Product NDC: 49349-031
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075468
Marketing Category: ANDA
Start Marketing Date: 20100922

Package Information of Clonazepam

Package NDC: 49349-031-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-031-02)

NDC Information of Clonazepam

NDC Code 49349-031-02
Proprietary Name Clonazepam
Package Description 30 TABLET in 1 BLISTER PACK (49349-031-02)
Product NDC 49349-031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonazepan
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100922
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CLONAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information