Package 76282-544-30

Brand: vilazodone hydrochloride

Generic: vilazodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76282-544-30
Digits Only 7628254430
Product NDC 76282-544
Product ID 76282-544_da0f5799-ae08-4f50-b909-96c73adeeb31
Description

30 TABLET, FILM COATED in 1 BOTTLE (76282-544-30)

Marketing

Marketing Status
Marketed Since 2022-12-01
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": "da0f5799-ae08-4f50-b909-96c73adeeb31", "openfda": {"upc": ["0376282545301", "0376282544304", "0376282546308"], "unii": ["U8HTX2GK8J"], "rxcui": ["1086772", "1086778", "1086784"], "spl_set_id": ["d1d8b51c-823b-4702-a726-a7530abd8957"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76282-544-30)", "package_ndc": "76282-544-30", "marketing_start_date": "20221201"}], "brand_name": "Vilazodone Hydrochloride", "product_id": "76282-544_da0f5799-ae08-4f50-b909-96c73adeeb31", "dosage_form": "TABLET, FILM COATED", "product_ndc": "76282-544", "generic_name": "Vilazodone Hydrochloride", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vilazodone Hydrochloride", "active_ingredients": [{"name": "VILAZODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208200", "marketing_category": "ANDA", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}