Package 85509-1495-6

{"route": ["ORAL"], "spl_id": "4b97c5af-891e-98f4-e063-6394a90ab4ea", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["47d18804-d8d6-8248-e063-6394a90a48a9"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85509-1495-3)", "package_ndc": "85509-1495-3", "marketing_start_date": "20260107"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85509-1495-6)", "package_ndc": "85509-1495-6", "marketing_start_date": "20260107"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85509-1495-9)", "package_ndc": "85509-1495-9", "marketing_start_date": "20260107"}], "brand_name": "Naproxen sodium", "product_id": "85509-1495_4b97c5af-891e-98f4-e063-6394a90ab4ea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "85509-1495", "generic_name": "Naproxen sodium", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "550 mg/1"}], "application_number": "ANDA078486", "marketing_category": "ANDA", "marketing_start_date": "20160426", "listing_expiration_date": "20271231"}