Package 23155-001-10

{"route": ["ORAL"], "spl_id": "e092716d-6522-4cfb-8728-622f9b553ef1", "openfda": {"upc": ["0323155003017", "0323155004014", "0323155002010"], "unii": ["FD171B778Y"], "rxcui": ["905199", "905222", "905225", "905395"], "spl_set_id": ["a04eefaf-ba3c-448d-8ece-4aa9ab2e3508"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (23155-001-01)", "package_ndc": "23155-001-01", "marketing_end_date": "20260831", "marketing_start_date": "20070406"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (23155-001-10)", "package_ndc": "23155-001-10", "marketing_end_date": "20260831", "marketing_start_date": "20070406"}], "brand_name": "HYDRALAZINE HYDROCHLORIDE", "product_id": "23155-001_e092716d-6522-4cfb-8728-622f9b553ef1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "23155-001", "generic_name": "hydralazine hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDRALAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDRALAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA086242", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20070406"}