Package 67386-421-01
Brand: xenazine
Generic: tetrabenazinePackage Facts
Identity
Package NDC
67386-421-01
Digits Only
6738642101
Product NDC
67386-421
Description
112 TABLET in 1 BOTTLE (67386-421-01)
Marketing
Marketing Status
Brand
xenazine
Generic
tetrabenazine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6f524695-2fc1-4c54-9212-69cff22cdfa7", "openfda": {"nui": ["N0000190856", "N0000190855"], "unii": ["Z9O08YRN8O"], "rxcui": ["199592", "805462", "805464", "805466"], "spl_set_id": ["ac768bab-8afa-4446-bc7f-caeeffec0cda"], "pharm_class_epc": ["Vesicular Monoamine Transporter 2 Inhibitor [EPC]"], "pharm_class_moa": ["Vesicular Monoamine Transporter 2 Inhibitors [MoA]"], "manufacturer_name": ["Lundbeck Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "112 TABLET in 1 BOTTLE (67386-421-01)", "package_ndc": "67386-421-01", "marketing_start_date": "20081124"}], "brand_name": "Xenazine", "product_id": "67386-421_6f524695-2fc1-4c54-9212-69cff22cdfa7", "dosage_form": "TABLET", "pharm_class": ["Vesicular Monoamine Transporter 2 Inhibitor [EPC]", "Vesicular Monoamine Transporter 2 Inhibitors [MoA]"], "product_ndc": "67386-421", "generic_name": "tetrabenazine", "labeler_name": "Lundbeck Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xenazine", "active_ingredients": [{"name": "TETRABENAZINE", "strength": "12.5 mg/1"}], "application_number": "NDA021894", "marketing_category": "NDA", "marketing_start_date": "20081124", "listing_expiration_date": "20261231"}