Package 72603-621-01

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72603-621-01
Digits Only 7260362101
Product NDC 72603-621
Product ID 72603-621_10a88607-0b5e-4707-b0cb-40c58a5c6774
Description

30 TABLET, FILM COATED in 1 BOTTLE (72603-621-01)

Marketing

Marketing Status
Marketed Since 2025-04-08
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": "10a88607-0b5e-4707-b0cb-40c58a5c6774", "openfda": {"upc": ["0372603621013", "0372603622010", "0372603623017", "0372603624014"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1431235"], "spl_set_id": ["10a88607-0b5e-4707-b0cb-40c58a5c6774"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72603-621-01)", "package_ndc": "72603-621-01", "marketing_start_date": "20250408"}], "brand_name": "lurasidone hydrochloride", "product_id": "72603-621_10a88607-0b5e-4707-b0cb-40c58a5c6774", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72603-621", "generic_name": "lurasidone hydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA212124", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}