Package 70771-1737-4

{"route": ["ORAL"], "spl_id": "b82674a0-84e9-4431-9041-e5c360bbdaca", "openfda": {"unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["0f5f8228-1304-4981-8577-029136627260"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (70771-1737-1)", "package_ndc": "70771-1737-1", "marketing_start_date": "20230201"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (70771-1737-3)", "package_ndc": "70771-1737-3", "marketing_start_date": "20230201"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1737-4)  / 10 TABLET, COATED in 1 BLISTER PACK (70771-1737-2)", "package_ndc": "70771-1737-4", "marketing_start_date": "20230201"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (70771-1737-5)", "package_ndc": "70771-1737-5", "marketing_start_date": "20230201"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (70771-1737-9)", "package_ndc": "70771-1737-9", "marketing_start_date": "20230201"}], "brand_name": "Lurasidone hydrochloride", "product_id": "70771-1737_b82674a0-84e9-4431-9041-e5c360bbdaca", "dosage_form": "TABLET, COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70771-1737", "generic_name": "Lurasidone hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA208052", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}