Package 50090-7170-0

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7170-0
Digits Only 5009071700
Product NDC 50090-7170
Product ID 50090-7170_d5b325d2-1204-4adb-b105-0bd981f990dc
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-7170-0)

Marketing

Marketing Status
Marketed Since 2024-05-15
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": "d5b325d2-1204-4adb-b105-0bd981f990dc", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1235247"], "spl_set_id": ["c96cbfc9-773b-410a-ada3-2822cbd58f8f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7170-0)", "package_ndc": "50090-7170-0", "marketing_start_date": "20240515"}], "brand_name": "lurasidone hydrochloride", "product_id": "50090-7170_d5b325d2-1204-4adb-b105-0bd981f990dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-7170", "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": "ANDA212244", "marketing_category": "ANDA", "marketing_start_date": "20230104", "listing_expiration_date": "20261231"}