Package 76282-523-30
Brand: lurasidone hydrochloride
Generic: lurasidone hydrochloridePackage Facts
Identity
Package NDC
76282-523-30
Digits Only
7628252330
Product NDC
76282-523
Description
30 TABLET, FILM COATED in 1 BOTTLE (76282-523-30)
Marketing
Marketing Status
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": "a2a08e69-a40e-48d5-af27-419093cfd9b0", "openfda": {"upc": ["0376282525303", "0376282524306", "0376282523309", "0376282534305", "0376282522302"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["4223e7f8-acbb-4738-9b77-ddc3405afb25"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76282-523-30)", "package_ndc": "76282-523-30", "marketing_start_date": "20230220"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "76282-523_a2a08e69-a40e-48d5-af27-419093cfd9b0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "76282-523", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208028", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}