Package 31722-519-05

{"route": ["ORAL"], "spl_id": "30381b85-deb3-bc70-e063-6294a90ad921", "openfda": {"upc": ["0331722519014", "0331722521017", "0331722522014", "0331722520010"], "unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["5da36930-d3da-4b5c-9e22-2b141bc01a9c"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-519-01)", "package_ndc": "31722-519-01", "marketing_start_date": "20100101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-519-05)", "package_ndc": "31722-519-05", "marketing_start_date": "20100101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (31722-519-10)", "package_ndc": "31722-519-10", "marketing_start_date": "20100101"}], "brand_name": "Hydralazine Hydrochloride", "product_id": "31722-519_30381b85-deb3-bc70-e063-6294a90ad921", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "31722-519", "generic_name": "Hydralazine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydralazine Hydrochloride", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040901", "marketing_category": "ANDA", "marketing_start_date": "20100101", "listing_expiration_date": "20261231"}