Package 43598-351-30

{"route": ["ORAL"], "spl_id": "f3c17d88-383d-89de-d8d6-8ed1bb1b3750", "openfda": {"upc": ["0343598353302", "0343598354309", "0343598351308", "0343598352305"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1431235"], "spl_set_id": ["9b512af1-98ab-1242-10e8-9534a002306e"], "manufacturer_name": ["Dr. Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43598-351-05)", "package_ndc": "43598-351-05", "marketing_start_date": "20230220"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43598-351-30)", "package_ndc": "43598-351-30", "marketing_start_date": "20230220"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (43598-351-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-351-79)", "package_ndc": "43598-351-78", "marketing_start_date": "20230220"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (43598-351-90)", "package_ndc": "43598-351-90", "marketing_start_date": "20230220"}], "brand_name": "Lurasidone hydrochloride", "product_id": "43598-351_f3c17d88-383d-89de-d8d6-8ed1bb1b3750", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43598-351", "generic_name": "Lurasidone hydrochloride", "labeler_name": "Dr. Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208047", "marketing_category": "ANDA", "marketing_start_date": "20230220", "listing_expiration_date": "20261231"}