Package 82804-215-30

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82804-215-30
Digits Only 8280421530
Product NDC 82804-215
Product ID 82804-215_fa9f0d28-c525-4a1e-acec-84c82e10b9a2
Description

30 TABLET in 1 BOTTLE (82804-215-30)

Marketing

Marketing Status
Marketed Since 2025-03-31
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

LURASIDONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fa9f0d28-c525-4a1e-acec-84c82e10b9a2", "openfda": {"upc": ["0382804215300"], "unii": ["O0P4I5851I"], "rxcui": ["1235247"], "spl_set_id": ["fa9f0d28-c525-4a1e-acec-84c82e10b9a2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-215-30)", "package_ndc": "82804-215-30", "marketing_start_date": "20250331"}], "brand_name": "LURASIDONE HYDROCHLORIDE", "product_id": "82804-215_fa9f0d28-c525-4a1e-acec-84c82e10b9a2", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "82804-215", "generic_name": "LURASIDONE HYDROCHLORIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LURASIDONE HYDROCHLORIDE", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208045", "marketing_category": "ANDA", "marketing_start_date": "20230310", "listing_expiration_date": "20261231"}