Package 71335-2721-2

{"route": ["ORAL"], "spl_id": "95a194c4-ed0a-4847-8722-30b3e5dff9dd", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["2bf66203-8b45-475d-9a70-4d7c8bdfe6b3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "8 TABLET, COATED in 1 BOTTLE (71335-2721-1)", "package_ndc": "71335-2721-1", "marketing_start_date": "20250926"}, {"sample": false, "description": "84 TABLET, COATED in 1 BOTTLE (71335-2721-2)", "package_ndc": "71335-2721-2", "marketing_start_date": "20250926"}, {"sample": false, "description": "56 TABLET, COATED in 1 BOTTLE (71335-2721-3)", "package_ndc": "71335-2721-3", "marketing_start_date": "20250926"}, {"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (71335-2721-4)", "package_ndc": "71335-2721-4", "marketing_start_date": "20250926"}], "brand_name": "Tramadol Hydrochloride", "product_id": "71335-2721_95a194c4-ed0a-4847-8722-30b3e5dff9dd", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-2721", "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": "50 mg/1"}], "application_number": "ANDA208708", "marketing_category": "ANDA", "marketing_start_date": "20230724", "listing_expiration_date": "20261231"}