Clonazepam - 76237-138-39 - (Clonazepam)

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Drug Information of Clonazepam

Product NDC: 76237-138
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: 76237-138
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074869
Marketing Category: ANDA
Start Marketing Date: 20111011

Package Information of Clonazepam

Package NDC: 76237-138-39
Package Description: 30 TABLET in 1 BLISTER PACK (76237-138-39)

NDC Information of Clonazepam

NDC Code 76237-138-39
Proprietary Name Clonazepam
Package Description 30 TABLET in 1 BLISTER PACK (76237-138-39)
Product NDC 76237-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111011
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name CLONAZEPAM
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Clonazepam


General Information