Package 71335-9670-4

{"route": ["ORAL"], "spl_id": "14c82d58-57d2-4128-894c-01f65528d5af", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833713"], "spl_set_id": ["acd5d8e0-a4cc-4654-ae04-faff347a60ca"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-1)", "package_ndc": "71335-9670-1", "marketing_start_date": "20230324"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-2)", "package_ndc": "71335-9670-2", "marketing_start_date": "20240403"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-3)", "package_ndc": "71335-9670-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-4)", "package_ndc": "71335-9670-4", "marketing_start_date": "20240403"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "71335-9670_14c82d58-57d2-4128-894c-01f65528d5af", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-9670", "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": "300 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20140819", "listing_expiration_date": "20261231"}