Package 0904-7423-46

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7423-46
Digits Only 0904742346
Product NDC 0904-7423
Description

30 TABLET, FILM COATED in 1 BOTTLE (0904-7423-46)

Marketing

Marketing Status
Marketed Since 2024-01-05
Brand lurasidone hydrochloride
Generic lurasidone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cecfd4c8-bff3-44fa-b360-b3e8a8e955f5", "openfda": {"upc": ["0309047422463", "0309047423460", "0309047424467", "0309047425464", "0309047421466"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["cecfd4c8-bff3-44fa-b360-b3e8a8e955f5"], "manufacturer_name": ["MAJOR PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0904-7423-46)", "package_ndc": "0904-7423-46", "marketing_start_date": "20240105"}], "brand_name": "lurasidone hydrochloride", "product_id": "0904-7423_cecfd4c8-bff3-44fa-b360-b3e8a8e955f5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-7423", "generic_name": "lurasidone hydrochloride", "labeler_name": "MAJOR PHARMACEUTICALS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA208037", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20261231"}