Package 0093-5503-56

{"route": ["ORAL"], "spl_id": "49dfc18c-9d68-4489-83f5-d59bb2596b80", "openfda": {"nui": ["N0000175430"], "upc": ["0300935506562", "0300935503561", "0300935505565", "0300935507569", "0300935504568"], "unii": ["N7U69T4SZR", "I9W7N6B1KJ"], "rxcui": ["403969", "403970", "403971", "403972", "721787"], "spl_set_id": ["3c28cf18-01a3-468a-ab3e-8aa82f918251"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (0093-5503-56)", "package_ndc": "0093-5503-56", "marketing_start_date": "20130410"}], "brand_name": "Olanzapine and Fluoxetine", "product_id": "0093-5503_49dfc18c-9d68-4489-83f5-d59bb2596b80", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0093-5503", "generic_name": "Olanzapine and Fluoxetine", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine and Fluoxetine", "active_ingredients": [{"name": "FLUOXETINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "OLANZAPINE", "strength": "3 mg/1"}], "application_number": "ANDA202074", "marketing_category": "ANDA", "marketing_start_date": "20130410", "listing_expiration_date": "20261231"}