Package 0378-0351-01

{"route": ["ORAL"], "spl_id": "6c9cb993-d2d8-4c2a-b425-1ce8867c970c", "openfda": {"nui": ["N0000180182"], "upc": ["0303780351011"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["c559b0b0-4087-d12a-e718-c18ccb6811e6"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0378-0351-01)", "package_ndc": "0378-0351-01", "marketing_start_date": "19860610"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0378-0351-10)", "package_ndc": "0378-0351-10", "marketing_start_date": "19860610"}], "brand_name": "Haloperidol", "product_id": "0378-0351_6c9cb993-d2d8-4c2a-b425-1ce8867c970c", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0378-0351", "generic_name": "haloperidol", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": ".5 mg/1"}], "application_number": "ANDA070278", "marketing_category": "ANDA", "marketing_start_date": "19860610", "listing_expiration_date": "20261231"}