Package 16714-891-01

{"route": ["ORAL"], "spl_id": "c5920565-605b-45cb-8da9-4d418ec3b356", "openfda": {"upc": ["0316714891019"], "unii": ["9TN87S3A3C", "J8BDZ68989"], "rxcui": ["849450"], "spl_set_id": ["3f2ec27e-0e96-4028-a1fa-114e6d501464"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (16714-891-01)", "package_ndc": "16714-891-01", "marketing_start_date": "20181127"}], "brand_name": "Sumatriptan and Naproxen Sodium", "product_id": "16714-891_c5920565-605b-45cb-8da9-4d418ec3b356", "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": "16714-891", "generic_name": "Sumatriptan and Naproxen Sodium", "labeler_name": "NorthStar RxLLC", "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": "20181127", "listing_expiration_date": "20261231"}