Package 0904-7358-61

Brand: lurasidone hydrochloride

Generic: lurasidone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7358-61
Digits Only 0904735861
Product NDC 0904-7358
Product ID 0904-7358_382b3af6-5685-44e2-b310-76fee0d2e0da
Description

100 BLISTER PACK in 1 CARTON (0904-7358-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

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": "382b3af6-5685-44e2-b310-76fee0d2e0da", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["d8b9ba36-fb02-4f52-b0ed-7fdd81d50c4c"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7358-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7358-61", "marketing_start_date": "20230220"}], "brand_name": "lurasidone hydrochloride", "product_id": "0904-7358_382b3af6-5685-44e2-b310-76fee0d2e0da", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "0904-7358", "generic_name": "lurasidone hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA212244", "marketing_category": "ANDA", "marketing_start_date": "20230104", "listing_expiration_date": "20261231"}