Package 59762-3721-3

{"route": ["ORAL"], "spl_id": "0deddc26-2764-4879-a0e4-a29fff246244", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["13930c94-d83a-414f-be35-b1fef35f738d"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59762-3721-1)", "package_ndc": "59762-3721-1", "marketing_start_date": "19811016"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59762-3721-3)", "package_ndc": "59762-3721-3", "marketing_start_date": "19811016"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59762-3721-4)", "package_ndc": "59762-3721-4", "marketing_start_date": "19811016"}], "brand_name": "Alprazolam", "product_id": "59762-3721_0deddc26-2764-4879-a0e4-a29fff246244", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "59762-3721", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19811016", "listing_expiration_date": "20261231"}