Package 23155-749-05

{"route": ["ORAL"], "spl_id": "c1d00e26-e74a-43a7-b418-88a61e816cfa", "openfda": {"upc": ["0323155749014", "0323155752014", "0323155751017"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["910dac3a-728c-4f94-a514-e2b8f4680d39"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-749-01)", "package_ndc": "23155-749-01", "marketing_start_date": "20220820"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-749-05)", "package_ndc": "23155-749-05", "marketing_start_date": "20220820"}], "brand_name": "Benazepril Hydrochloride", "product_id": "23155-749_c1d00e26-e74a-43a7-b418-88a61e816cfa", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "23155-749", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076267", "marketing_category": "ANDA", "marketing_start_date": "20220820", "listing_expiration_date": "20261231"}