Package 71335-0267-2

{"route": ["ORAL"], "spl_id": "80b5095b-d8b3-4b21-8ef7-97be51391ea2", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["08bc0034-3b33-47d8-aec2-b36535ac85a2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-0267-1)", "package_ndc": "71335-0267-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71335-0267-2)", "package_ndc": "71335-0267-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71335-0267-3)", "package_ndc": "71335-0267-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-0267-4)", "package_ndc": "71335-0267-4", "marketing_start_date": "20220209"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-0267_80b5095b-d8b3-4b21-8ef7-97be51391ea2", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-0267", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}