Package 65862-954-30

{"route": ["ORAL"], "spl_id": "b73e1972-e96d-4463-ad39-f7bed99466e9", "openfda": {"upc": ["0365862955302", "0365862956309"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["b3e9cc86-0c5c-444f-ab57-f4d1a6865035"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (65862-954-05)", "package_ndc": "65862-954-05", "marketing_start_date": "20230310"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-954-30)", "package_ndc": "65862-954-30", "marketing_start_date": "20230310"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65862-954-90)", "package_ndc": "65862-954-90", "marketing_start_date": "20230310"}], "brand_name": "LURASIDONE HYDROCHLORIDE", "product_id": "65862-954_b73e1972-e96d-4463-ad39-f7bed99466e9", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "65862-954", "generic_name": "LURASIDONE HYDROCHLORIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LURASIDONE HYDROCHLORIDE", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA208045", "marketing_category": "ANDA", "marketing_start_date": "20230310", "listing_expiration_date": "20261231"}