Package 71335-9756-5

{"route": ["ORAL"], "spl_id": "b9ddda4a-9598-451d-abb2-f13f4ba4e67f", "openfda": {"unii": ["FD171B778Y"], "rxcui": ["905395"], "spl_set_id": ["62475f78-5410-43c2-a11d-54a8363c3ae1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9756-1)", "package_ndc": "71335-9756-1", "marketing_start_date": "20230725"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9756-2)", "package_ndc": "71335-9756-2", "marketing_start_date": "20230725"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-9756-3)", "package_ndc": "71335-9756-3", "marketing_start_date": "20230725"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9756-4)", "package_ndc": "71335-9756-4", "marketing_start_date": "20230725"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-9756-5)", "package_ndc": "71335-9756-5", "marketing_start_date": "20230725"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "71335-9756_b9ddda4a-9598-451d-abb2-f13f4ba4e67f", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "71335-9756", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA205236", "marketing_category": "ANDA", "marketing_start_date": "20170526", "listing_expiration_date": "20261231"}