Package 71335-1365-1

{"route": ["ORAL"], "spl_id": "d05a4467-7d16-41ef-b1d4-25a4b96382f2", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["58977ec4-36ea-4d81-a8f0-7298425cbc84"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1)", "package_ndc": "71335-1365-1", "marketing_start_date": "20200213"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2)", "package_ndc": "71335-1365-2", "marketing_start_date": "20191007"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3)", "package_ndc": "71335-1365-3", "marketing_start_date": "20240530"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4)", "package_ndc": "71335-1365-4", "marketing_start_date": "20200311"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-1365_d05a4467-7d16-41ef-b1d4-25a4b96382f2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-1365", "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": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}