Package 80425-0492-2

{"route": ["ORAL"], "spl_id": "2d325eb5-e49e-6529-e063-6294a90a5cc1", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["2d324cb1-8567-55e5-e063-6294a90aa5d9"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (80425-0492-1)", "package_ndc": "80425-0492-1", "marketing_start_date": "20250202"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0492-2)", "package_ndc": "80425-0492-2", "marketing_start_date": "20250202"}], "brand_name": "Ciprofloxacin", "product_id": "80425-0492_2d325eb5-e49e-6529-e063-6294a90a5cc1", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "80425-0492", "generic_name": "Ciprofolxacin", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA208921", "marketing_category": "ANDA", "marketing_start_date": "20250202", "listing_expiration_date": "20261231"}