Xenazine - 67386-421-01 - (tetrabenazine)

Alphabetical Index


Drug Information of Xenazine

Product NDC: 67386-421
Proprietary Name: Xenazine
Non Proprietary Name: tetrabenazine
Active Ingredient(s): 12.5    mg/1 & nbsp;   tetrabenazine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Xenazine

Product NDC: 67386-421
Labeler Name: Lundbeck Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021894
Marketing Category: NDA
Start Marketing Date: 20081124

Package Information of Xenazine

Package NDC: 67386-421-01
Package Description: 112 TABLET in 1 BOTTLE (67386-421-01)

NDC Information of Xenazine

NDC Code 67386-421-01
Proprietary Name Xenazine
Package Description 112 TABLET in 1 BOTTLE (67386-421-01)
Product NDC 67386-421
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tetrabenazine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081124
Marketing Category Name NDA
Labeler Name Lundbeck Inc.
Substance Name TETRABENAZINE
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Xenazine


General Information