Package 63629-8319-3

{"route": ["ORAL"], "spl_id": "60f605b4-94c6-4ffe-9b13-ba30fdc6a9b5", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["b2f3f007-6dda-4532-9f7f-d93f6e65254c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8319-1)", "package_ndc": "63629-8319-1", "marketing_start_date": "20200604"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8319-2)", "package_ndc": "63629-8319-2", "marketing_start_date": "20200514"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8319-3)", "package_ndc": "63629-8319-3", "marketing_start_date": "20201203"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8319-4)", "package_ndc": "63629-8319-4", "marketing_start_date": "20240403"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "63629-8319_60f605b4-94c6-4ffe-9b13-ba30fdc6a9b5", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-8319", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20140819", "listing_expiration_date": "20261231"}