Package 47335-410-88

{"route": ["ORAL"], "spl_id": "c67d3234-28c7-40a9-a472-87747bb4242a", "openfda": {"upc": ["0347335410228"], "unii": ["9TN87S3A3C", "J8BDZ68989"], "rxcui": ["849450"], "spl_set_id": ["96ed12a3-fa76-4afd-bee8-1ab19eb607f3"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (47335-410-22)", "package_ndc": "47335-410-22", "marketing_start_date": "20180720"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-410-83)", "package_ndc": "47335-410-83", "marketing_start_date": "20180720"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-410-88)", "package_ndc": "47335-410-88", "marketing_start_date": "20180720"}], "brand_name": "Sumatriptan and Naproxen Sodium", "product_id": "47335-410_c67d3234-28c7-40a9-a472-87747bb4242a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "47335-410", "generic_name": "Sumatriptan and Naproxen Sodium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan and Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "500 mg/1"}, {"name": "SUMATRIPTAN SUCCINATE", "strength": "85 mg/1"}], "application_number": "ANDA202803", "marketing_category": "ANDA", "marketing_start_date": "20180720", "listing_expiration_date": "20261231"}