Package 68788-7572-3

{"route": ["ORAL"], "spl_id": "afc77c85-efb4-4380-b745-1284d57ade68", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["20eb9d9f-11df-464f-a1b0-949f8fda4042"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-7572-2)", "package_ndc": "68788-7572-2", "marketing_start_date": "20191227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7572-3)", "package_ndc": "68788-7572-3", "marketing_start_date": "20191227"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68788-7572-4)", "package_ndc": "68788-7572-4", "marketing_start_date": "20191227"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7572-6)", "package_ndc": "68788-7572-6", "marketing_start_date": "20191227"}], "brand_name": "Naproxen", "product_id": "68788-7572_afc77c85-efb4-4380-b745-1284d57ade68", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-7572", "generic_name": "Naproxen Sodium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}