Package 21130-062-09

{"route": ["ORAL"], "spl_id": "4650a28b-d299-a5e5-e063-6294a90ad9f7", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f2a273f8-d623-dc2f-e053-2995a90a0c02"], "manufacturer_name": ["Safeway, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (21130-062-05)", "package_ndc": "21130-062-05", "marketing_start_date": "20230830"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (21130-062-09)", "package_ndc": "21130-062-09", "marketing_start_date": "20230830"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (21130-062-20)", "package_ndc": "21130-062-20", "marketing_start_date": "20230930"}], "brand_name": "Naproxen", "product_id": "21130-062_4650a28b-d299-a5e5-e063-6294a90ad9f7", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-062", "generic_name": "Naproxen", "labeler_name": "Safeway, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20230830", "listing_expiration_date": "20261231"}