Package 72789-151-06

{"route": ["ORAL"], "spl_id": "3ca57d28-5c7a-40fe-e063-6394a90a690b", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0372789151304"], "unii": ["YU55MQ3IZY"], "rxcui": ["308047"], "spl_set_id": ["4203d3fe-916e-41af-9daf-f58f4fed6f9c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (72789-151-06)", "package_ndc": "72789-151-06", "marketing_start_date": "20221111"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-151-30)", "package_ndc": "72789-151-30", "marketing_start_date": "20221231"}], "brand_name": "Alprazolam", "product_id": "72789-151_3ca57d28-5c7a-40fe-e063-6394a90a690b", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72789-151", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}