Package 71335-1925-1

{"route": ["ORAL"], "spl_id": "5106647a-1c82-4ebe-95f3-db46fb2398db", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849398"], "spl_set_id": ["1c2325f7-1d65-429d-a64d-6ab075df1c20"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1925-1)", "package_ndc": "71335-1925-1", "marketing_start_date": "20250130"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1925-2)", "package_ndc": "71335-1925-2", "marketing_start_date": "20250130"}, {"sample": false, "description": "42 TABLET, FILM COATED in 1 BOTTLE (71335-1925-3)", "package_ndc": "71335-1925-3", "marketing_start_date": "20250130"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1925-4)", "package_ndc": "71335-1925-4", "marketing_start_date": "20250130"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-1925-5)", "package_ndc": "71335-1925-5", "marketing_start_date": "20250130"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1925-6)", "package_ndc": "71335-1925-6", "marketing_start_date": "20210729"}], "brand_name": "Naproxen Sodium", "product_id": "71335-1925_5106647a-1c82-4ebe-95f3-db46fb2398db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-1925", "generic_name": "Naproxen Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "275 mg/1"}], "application_number": "ANDA200629", "marketing_category": "ANDA", "marketing_start_date": "20111031", "listing_expiration_date": "20271231"}