Package 68788-8462-2

{"route": ["ORAL"], "spl_id": "7f88e44d-2f31-44c6-8d56-fdca3da40626", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589"], "spl_set_id": ["6dcbb5e9-1e8f-4069-9244-adb46356714d"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (68788-8462-2)", "package_ndc": "68788-8462-2", "marketing_start_date": "20230621"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68788-8462-3)", "package_ndc": "68788-8462-3", "marketing_start_date": "20230621"}], "brand_name": "Diazepam", "product_id": "68788-8462_7f88e44d-2f31-44c6-8d56-fdca3da40626", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68788-8462", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "10 mg/1"}], "application_number": "ANDA070325", "marketing_category": "ANDA", "marketing_start_date": "20230621", "listing_expiration_date": "20261231"}