Package 50844-417-14

{"route": ["ORAL"], "spl_id": "89d3ed35-e75c-41d8-aa99-57cc1fd866d2", "openfda": {"upc": ["0050844604063", "0050844417168"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["717518e4-2537-4229-b765-c6acfe963d4b"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 POUCH in 1 CARTON (50844-417-11)  / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)", "package_ndc": "50844-417-11", "marketing_start_date": "20170201"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-14)", "package_ndc": "50844-417-14", "marketing_start_date": "20170201"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-16)", "package_ndc": "50844-417-16", "marketing_start_date": "20170201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-417-19)  / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-417-19", "marketing_start_date": "20170201"}, {"sample": false, "description": "48 POUCH in 1 CARTON (50844-417-22)  / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43)", "package_ndc": "50844-417-22", "marketing_start_date": "20170201"}, {"sample": false, "description": "25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-56)", "package_ndc": "50844-417-56", "marketing_start_date": "20170201"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-98)", "package_ndc": "50844-417-98", "marketing_start_date": "20170201"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-417-99)", "package_ndc": "50844-417-99", "marketing_start_date": "20170201"}], "brand_name": "Naproxen Sodium", "product_id": "50844-417_89d3ed35-e75c-41d8-aa99-57cc1fd866d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50844-417", "generic_name": "Naproxen Sodium", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20170201", "listing_expiration_date": "20271231"}