Package 0363-6099-01

{"route": ["ORAL"], "spl_id": "13b172b6-b829-8fe5-e063-6294a90a37e3", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["8771300f-e907-3d53-e053-2a95a90ae402"], "manufacturer_name": ["WALGREENS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (0363-6099-01)", "package_ndc": "0363-6099-01", "marketing_start_date": "20190708"}, {"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (0363-6099-05)", "package_ndc": "0363-6099-05", "marketing_start_date": "20190708"}, {"sample": false, "description": "200 TABLET, COATED in 1 BOTTLE (0363-6099-20)", "package_ndc": "0363-6099-20", "marketing_start_date": "20190708"}], "brand_name": "ALL DAY PAIN RELIEF", "product_id": "0363-6099_13b172b6-b829-8fe5-e063-6294a90a37e3", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-6099", "generic_name": "NAPROXEN SODIUM", "labeler_name": "WALGREENS", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ALL DAY PAIN RELIEF", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20190630", "listing_expiration_date": "20261231"}