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Xenazine
Xenazine - 67386-421-01 - (tetrabenazine)
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 |
