Package 68788-7161-9

{"route": ["ORAL"], "spl_id": "30d1e6c7-87dc-45b2-a999-00ca06ee0ccd", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078"], "spl_set_id": ["5bded04a-d848-4ac6-b7c3-ff9b9fef3d29"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7161-3)", "package_ndc": "68788-7161-3", "marketing_start_date": "20180605"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7161-6)", "package_ndc": "68788-7161-6", "marketing_start_date": "20180605"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7161-9)", "package_ndc": "68788-7161-9", "marketing_start_date": "20180605"}], "brand_name": "Olanzapine", "product_id": "68788-7161_30d1e6c7-87dc-45b2-a999-00ca06ee0ccd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68788-7161", "generic_name": "Olanzapine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "5 mg/1"}], "application_number": "ANDA202862", "marketing_category": "ANDA", "marketing_start_date": "20180605", "listing_expiration_date": "20261231"}