Package 47335-685-81

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 47335-685-81
Digits Only 4733568581
Product NDC 47335-685
Product ID 47335-685_2ebf334e-6f66-4ef7-b0ca-9d21ccb3165e
Description

90 TABLET in 1 BOTTLE (47335-685-81)

Marketing

Marketing Status
Marketed Since 2023-02-20
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": "2ebf334e-6f66-4ef7-b0ca-9d21ccb3165e", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["6d97d871-66d3-4ed8-bbc5-0620e9f69ae5"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (47335-685-13)", "package_ndc": "47335-685-13", "marketing_start_date": "20230220"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (47335-685-81)", "package_ndc": "47335-685-81", "marketing_start_date": "20230220"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (47335-685-83)", "package_ndc": "47335-685-83", "marketing_start_date": "20230220"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "47335-685_2ebf334e-6f66-4ef7-b0ca-9d21ccb3165e", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "47335-685", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA208066", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}