Package 69097-982-02

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69097-982-02
Digits Only 6909798202
Product NDC 69097-982
Product ID 69097-982_e16f2d8b-a5ec-498f-97c4-d1c9d897140f
Description

30 TABLET, FILM COATED in 1 BOTTLE (69097-982-02)

Marketing

Marketing Status
Marketed Since 2023-01-23
Brand vilazodone hydrochloride
Generic vilazodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Vilazodone Hydrochloride, Vilazodone hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e16f2d8b-a5ec-498f-97c4-d1c9d897140f", "openfda": {"upc": ["0369097981020", "0369097979027", "0369097982027"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["658c4bc1-4128-4e0e-8852-b5f68880e8d7"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69097-982-02)", "package_ndc": "69097-982-02", "marketing_start_date": "20230123"}], "brand_name": "Vilazodone hydrochloride", "product_id": "69097-982_e16f2d8b-a5ec-498f-97c4-d1c9d897140f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69097-982", "generic_name": "Vilazodone hydrochloride", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208200", "marketing_category": "ANDA", "marketing_start_date": "20230123", "listing_expiration_date": "20261231"}