Onfi - 67386-310-01 - (clobazam)

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Drug Information of Onfi

Product NDC: 67386-310
Proprietary Name: Onfi
Non Proprietary Name: clobazam
Active Ingredient(s): 5    mg/1 & nbsp;   clobazam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Onfi

Product NDC: 67386-310
Labeler Name: Lundbeck LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA202067
Marketing Category: NDA
Start Marketing Date: 20111021

Package Information of Onfi

Package NDC: 67386-310-01
Package Description: 1 BOTTLE in 1 CARTON (67386-310-01) > 100 TABLET in 1 BOTTLE

NDC Information of Onfi

NDC Code 67386-310-01
Proprietary Name Onfi
Package Description 1 BOTTLE in 1 CARTON (67386-310-01) > 100 TABLET in 1 BOTTLE
Product NDC 67386-310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clobazam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111021
Marketing Category Name NDA
Labeler Name Lundbeck LLC
Substance Name CLOBAZAM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient],Cytochrome P450 2D6 Inhibitors [MoA]

Complete Information of Onfi


General Information