Package 71335-1676-2

{"route": ["ORAL"], "spl_id": "6da94891-d49c-4fab-ba67-1a585a385be9", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833711"], "spl_set_id": ["66359f41-9999-4cb8-b632-1fe2ec1e60b2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-1)", "package_ndc": "71335-1676-1", "marketing_start_date": "20200710"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-2)", "package_ndc": "71335-1676-2", "marketing_start_date": "20200708"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-3)", "package_ndc": "71335-1676-3", "marketing_start_date": "20200813"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-4)", "package_ndc": "71335-1676-4", "marketing_start_date": "20240404"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "71335-1676_6da94891-d49c-4fab-ba67-1a585a385be9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1676", "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": "ANDA201384", "marketing_category": "ANDA", "marketing_start_date": "20111212", "listing_expiration_date": "20261231"}