Package 49884-250-11

{"route": ["ORAL"], "spl_id": "c2eef390-8690-4148-ac37-45e392be15a6", "openfda": {"nui": ["N0000175430"], "upc": ["0349884253110", "0349884277116", "0349884250119", "0349884251116", "0349884252113"], "unii": ["N7U69T4SZR", "I9W7N6B1KJ"], "rxcui": ["403969", "403970", "403971", "403972", "721787"], "spl_set_id": ["2f6ceda3-3edc-4427-98a6-23e3c930c44d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (49884-250-11)", "package_ndc": "49884-250-11", "marketing_start_date": "20121126"}], "brand_name": "Olanzapine and Fluoxetine", "product_id": "49884-250_c2eef390-8690-4148-ac37-45e392be15a6", "dosage_form": "CAPSULE", "pharm_class": ["Atypical Antipsychotic [EPC]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "49884-250", "generic_name": "olanzapine and fuoxetine", "labeler_name": "Endo 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": "6 mg/1"}], "application_number": "ANDA077742", "marketing_category": "ANDA", "marketing_start_date": "20121126", "listing_expiration_date": "20261231"}