Package 10135-753-10

{"route": ["ORAL"], "spl_id": "23e5e8d5-bddd-f9a9-e063-6394a90adb0c", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["e7a61604-741f-2d3b-e053-2995a90a62fc"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10135-753-01)", "package_ndc": "10135-753-01", "marketing_start_date": "20220801"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10135-753-10)", "package_ndc": "10135-753-10", "marketing_start_date": "20220801"}], "brand_name": "Haloperidol", "product_id": "10135-753_23e5e8d5-bddd-f9a9-e063-6394a90adb0c", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "10135-753", "generic_name": "Haloperidol", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "1 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}