Package 68788-8535-9

{"route": ["ORAL"], "spl_id": "4f1c703b-25a8-4b6d-953f-3782ff39b585", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160"], "spl_set_id": ["ff08b9ee-03bf-4f5b-930e-233a3b8866af"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BLISTER PACK (68788-8535-9)", "package_ndc": "68788-8535-9", "marketing_start_date": "20231023"}], "brand_name": "Sumatriptan", "product_id": "68788-8535_4f1c703b-25a8-4b6d-953f-3782ff39b585", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "68788-8535", "generic_name": "Sumatriptan", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20231023", "listing_expiration_date": "20261231"}