Package 0228-3086-06

{"route": ["ORAL"], "spl_id": "e89f9f55-9cd1-4b9d-b0a0-2d0480dd559c", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0302283083061"], "unii": ["YU55MQ3IZY"], "rxcui": ["433798", "433799", "433800", "433801"], "spl_set_id": ["a64496be-bf43-4ba9-a4b1-bd632965c1a0"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-3086-06)", "package_ndc": "0228-3086-06", "marketing_end_date": "20260731", "marketing_start_date": "20070312"}], "brand_name": "Alprazolam Extended Release", "product_id": "0228-3086_e89f9f55-9cd1-4b9d-b0a0-2d0480dd559c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0228-3086", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "3 mg/1"}], "application_number": "ANDA078056", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20070312"}