Package 82804-128-30

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-128-30
Digits Only 8280412830
Product NDC 82804-128
Description

30 TABLET in 1 BOTTLE (82804-128-30)

Marketing

Marketing Status
Marketed Since 2024-07-19
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": "f68720fd-9122-4922-b472-733da8bd0a00", "openfda": {"upc": ["0382804128303"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086784"], "spl_set_id": ["f68720fd-9122-4922-b472-733da8bd0a00"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-128-30)", "package_ndc": "82804-128-30", "marketing_start_date": "20240719"}], "brand_name": "vilazodone hydrochloride", "product_id": "82804-128_f68720fd-9122-4922-b472-733da8bd0a00", "dosage_form": "TABLET", "product_ndc": "82804-128", "generic_name": "vilazodone hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208228", "marketing_category": "ANDA", "marketing_start_date": "20231026", "listing_expiration_date": "20261231"}