Package 50090-6438-0

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-6438-0
Digits Only 5009064380
Product NDC 50090-6438
Product ID 50090-6438_6bf72f5b-ee22-47bb-a052-2bf67dde23a9
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-6438-0)

Marketing

Marketing Status
Marketed Since 2023-04-17
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6bf72f5b-ee22-47bb-a052-2bf67dde23a9", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1235247"], "spl_set_id": ["3cd2da15-4d51-4e5c-b683-1936dc19e234"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6438-0)", "package_ndc": "50090-6438-0", "marketing_start_date": "20230417"}], "brand_name": "lurasidone hydrochloride", "product_id": "50090-6438_6bf72f5b-ee22-47bb-a052-2bf67dde23a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-6438", "generic_name": "lurasidone hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208049", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}