Package 60505-3278-0

{"route": ["ORAL"], "spl_id": "997c6776-1ac1-bcb1-022c-2c5b6c277395", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312076", "314155", "351107", "351108"], "spl_set_id": ["96165590-b287-0ed9-3723-752af59aedad"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (60505-3278-0)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "60505-3278-0", "marketing_start_date": "20111024"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (60505-3278-3)", "package_ndc": "60505-3278-3", "marketing_start_date": "20111024"}, {"sample": false, "description": "1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (60505-3278-8)", "package_ndc": "60505-3278-8", "marketing_start_date": "20111024"}], "brand_name": "Olanzapine", "product_id": "60505-3278_997c6776-1ac1-bcb1-022c-2c5b6c277395", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60505-3278", "generic_name": "Olanzapine", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA091265", "marketing_category": "ANDA", "marketing_start_date": "20111024", "listing_expiration_date": "20261231"}