Package 16729-352-10
Brand: vilazodone hydrochloride
Generic: vilazodone hydrochloridePackage Facts
Identity
Package NDC
16729-352-10
Digits Only
1672935210
Product NDC
16729-352
Description
30 TABLET in 1 BOTTLE (16729-352-10)
Marketing
Marketing Status
Brand
vilazodone hydrochloride
Generic
vilazodone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40aa8e57-b9a0-9e45-e063-6294a90ab03e", "openfda": {"unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["f917f30d-f2a7-43eb-836f-53eaa2a31cb0"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (16729-352-10)", "package_ndc": "16729-352-10", "marketing_start_date": "20220604"}], "brand_name": "Vilazodone Hydrochloride", "product_id": "16729-352_40aa8e57-b9a0-9e45-e063-6294a90ab03e", "dosage_form": "TABLET", "product_ndc": "16729-352", "generic_name": "Vilazodone Hydrochloride", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone Hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208209", "marketing_category": "ANDA", "marketing_start_date": "20220604", "listing_expiration_date": "20261231"}