Package 83939-0002-2

{"route": ["ORAL"], "spl_id": "42543e8f-06f4-2b34-e063-6394a90a4abb", "openfda": {"unii": ["4BA73M5E37"], "rxcui": ["309309"], "spl_set_id": ["42542f65-84a7-fdab-e063-6394a90a1095"], "manufacturer_name": ["VERITYRX, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET, FILM COATED in 1 POUCH (83939-0002-1)", "package_ndc": "83939-0002-1", "marketing_start_date": "20251103"}, {"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (83939-0002-2)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "83939-0002-2", "marketing_start_date": "20251103"}, {"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (83939-0002-3)  / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "83939-0002-3", "marketing_start_date": "20251103"}], "brand_name": "Ciprofloxacin Hydrochloride", "product_id": "83939-0002_42543e8f-06f4-2b34-e063-6394a90a4abb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 1A2 Inhibitors [MoA]", "Fluoroquinolone Antibacterial [EPC]", "Fluoroquinolones [CS]"], "product_ndc": "83939-0002", "generic_name": "Ciprofloxacin Hydrochloride", "labeler_name": "VERITYRX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ciprofloxacin Hydrochloride", "active_ingredients": [{"name": "CIPROFLOXACIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA076593", "marketing_category": "ANDA", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}