Package 67877-640-05

{"route": ["ORAL"], "spl_id": "6e4065a5-2672-4ef4-996d-f9d2f58970d3", "openfda": {"upc": ["0367877639901", "0367877642055", "0367877640303"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040041", "1235247", "1297278", "1431235"], "spl_set_id": ["36b6bacd-ac11-493b-a8a4-8dad448ed9d5"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-640-05)", "package_ndc": "67877-640-05", "marketing_start_date": "20230104"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67877-640-30)", "package_ndc": "67877-640-30", "marketing_start_date": "20230104"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-640-38)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-640-33)", "package_ndc": "67877-640-38", "marketing_start_date": "20230104"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (67877-640-90)", "package_ndc": "67877-640-90", "marketing_start_date": "20230104"}], "brand_name": "lurasidone hydrochloride", "product_id": "67877-640_6e4065a5-2672-4ef4-996d-f9d2f58970d3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67877-640", "generic_name": "lurasidone hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lurasidone hydrochloride", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA212244", "marketing_category": "ANDA", "marketing_start_date": "20230104", "listing_expiration_date": "20261231"}