Package 0456-1110-30
Brand: viibryd
Generic: vilazodone hydrochloridePackage Facts
Identity
Package NDC
0456-1110-30
Digits Only
0456111030
Product NDC
0456-1110
Description
30 TABLET in 1 BOTTLE (0456-1110-30)
Marketing
Marketing Status
Brand
viibryd
Generic
vilazodone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7502bf82-6281-4d90-8471-1450580c4f3c", "openfda": {"upc": ["0304561120307", "0304561140305"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086776", "1086778", "1086780", "1086784", "1086786", "1086789", "1086790", "1653469", "1653470"], "spl_set_id": ["4c55ccfb-c4cf-11df-851a-0800200c9a66"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0456-1110-30)", "package_ndc": "0456-1110-30", "marketing_start_date": "20110429"}], "brand_name": "VIIBRYD", "product_id": "0456-1110_7502bf82-6281-4d90-8471-1450580c4f3c", "dosage_form": "TABLET", "product_ndc": "0456-1110", "generic_name": "vilazodone hydrochloride", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIIBRYD", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA022567", "marketing_category": "NDA", "marketing_start_date": "20110429", "listing_expiration_date": "20261231"}