Package 62332-234-30

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62332-234-30
Digits Only 6233223430
Product NDC 62332-234
Description

30 TABLET, FILM COATED in 1 BOTTLE (62332-234-30)

Marketing

Marketing Status
Marketed Since 2022-06-04
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": "d97cafa3-ede7-49c6-bba1-6414e6968cb5", "openfda": {"upc": ["0362332232307", "0362332234301"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["8b95b850-8bdf-4255-a691-783d1a94bd07"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-234-30)", "package_ndc": "62332-234-30", "marketing_start_date": "20220604"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-234-71)", "package_ndc": "62332-234-71", "marketing_start_date": "20220604"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-234-90)", "package_ndc": "62332-234-90", "marketing_start_date": "20220604"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-234-91)", "package_ndc": "62332-234-91", "marketing_start_date": "20220604"}], "brand_name": "VILAZODONE HYDROCHLORIDE", "product_id": "62332-234_d97cafa3-ede7-49c6-bba1-6414e6968cb5", "dosage_form": "TABLET, FILM COATED", "product_ndc": "62332-234", "generic_name": "VILAZODONE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VILAZODONE HYDROCHLORIDE", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208202", "marketing_category": "ANDA", "marketing_start_date": "20220604", "listing_expiration_date": "20261231"}