Package 79903-005-25

{"route": ["ORAL"], "spl_id": "7ff7ea22-53e8-4895-9960-c48a4bc4ad83", "openfda": {"upc": ["0194346189120"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["c4909e43-57ba-44bc-a234-a02cc884891c"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20)", "package_ndc": "79903-005-20", "marketing_start_date": "20201022"}, {"sample": false, "description": "225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25)", "package_ndc": "79903-005-25", "marketing_start_date": "20201022"}, {"sample": false, "description": "270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27)", "package_ndc": "79903-005-27", "marketing_start_date": "20201022"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90)", "package_ndc": "79903-005-90", "marketing_start_date": "20201022"}], "brand_name": "All Day Pain Relief", "product_id": "79903-005_7ff7ea22-53e8-4895-9960-c48a4bc4ad83", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-005", "generic_name": "Naproxen Sodium", "labeler_name": "WALMART INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20201022", "listing_expiration_date": "20261231"}