Package 80425-0496-2

{"route": ["ORAL"], "spl_id": "32c41fa1-f6d5-fe36-e063-6394a90a23bb", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197591"], "spl_set_id": ["2d322c6a-7f7e-1cc4-e063-6294a90a8e2e"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (80425-0496-1)", "package_ndc": "80425-0496-1", "marketing_start_date": "20250202"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (80425-0496-2)", "package_ndc": "80425-0496-2", "marketing_start_date": "20250202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (80425-0496-3)", "package_ndc": "80425-0496-3", "marketing_start_date": "20250202"}], "brand_name": "Diazepam", "product_id": "80425-0496_32c41fa1-f6d5-fe36-e063-6394a90a23bb", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "80425-0496", "dea_schedule": "CIV", "generic_name": "diazepam", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/1"}], "application_number": "ANDA070325", "marketing_category": "ANDA", "marketing_start_date": "20250202", "listing_expiration_date": "20261231"}