Package 65841-626-01

{"route": ["ORAL"], "spl_id": "2ff366f9-878f-4fcb-b2d4-00fb6e31ecbf", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["509d0eb2-b930-4836-9669-dbebf0ac4076"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65841-626-01)", "package_ndc": "65841-626-01", "marketing_start_date": "20080103"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65841-626-10)", "package_ndc": "65841-626-10", "marketing_start_date": "20080103"}], "brand_name": "Haloperidol", "product_id": "65841-626_2ff366f9-878f-4fcb-b2d4-00fb6e31ecbf", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "65841-626", "generic_name": "Haloperidol", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "5 mg/1"}], "application_number": "ANDA077580", "marketing_category": "ANDA", "marketing_start_date": "20080103", "listing_expiration_date": "20261231"}