Package 62332-495-90

{"route": ["ORAL"], "spl_id": "2ad2918d-7142-4425-bd00-45a269ef0d61", "openfda": {"upc": ["0362332496303"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["1cc441b3-0a23-4c68-a90e-436030b7daf2"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (62332-495-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "62332-495-10", "marketing_start_date": "20230124"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-495-30)", "package_ndc": "62332-495-30", "marketing_start_date": "20230124"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-495-71)", "package_ndc": "62332-495-71", "marketing_start_date": "20230124"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-495-90)", "package_ndc": "62332-495-90", "marketing_start_date": "20230124"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-495-91)", "package_ndc": "62332-495-91", "marketing_start_date": "20230124"}], "brand_name": "Lurasidone Hydrochloride", "product_id": "62332-495_2ad2918d-7142-4425-bd00-45a269ef0d61", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "62332-495", "generic_name": "Lurasidone Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone Hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA213248", "marketing_category": "ANDA", "marketing_start_date": "20230124", "listing_expiration_date": "20261231"}