Package 69848-010-05

{"route": ["ORAL"], "spl_id": "4690bf52-d225-e2ee-e063-6394a90ad8a9", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["8cb8030c-b281-315c-e053-2a95a90a36f0"], "manufacturer_name": ["Granules USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (69848-010-01)", "package_ndc": "69848-010-01", "marketing_start_date": "20190701"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (69848-010-05)", "package_ndc": "69848-010-05", "marketing_start_date": "20230301"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (69848-010-10)", "package_ndc": "69848-010-10", "marketing_start_date": "20230301"}], "brand_name": "Naproxen Sodium", "product_id": "69848-010_4690bf52-d225-e2ee-e063-6394a90ad8a9", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69848-010", "generic_name": "Naproxen Sodium", "labeler_name": "Granules USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}