Package 65862-928-36

{"route": ["ORAL"], "spl_id": "b0441826-19e2-4113-89b7-727a2b882a09", "openfda": {"unii": ["9TN87S3A3C", "J8BDZ68989"], "rxcui": ["849450"], "spl_set_id": ["f5203c66-0a40-4263-a237-b71e930e4697"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (65862-928-36)", "package_ndc": "65862-928-36", "marketing_start_date": "20180215"}], "brand_name": "Sumatriptan and Naproxen Sodium", "product_id": "65862-928_b0441826-19e2-4113-89b7-727a2b882a09", "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": "65862-928", "generic_name": "Sumatriptan and Naproxen Sodium", "labeler_name": "Aurobindo Pharma Limited", "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": "ANDA207457", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}