Package 65162-754-03

{"route": ["ORAL"], "spl_id": "1897ce48-56e1-415f-9db3-224c48b3063e", "openfda": {"upc": ["0365162751031", "0365162753035", "0365162754032", "0365162752038"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["a216253b-27cb-42ef-b5a8-67fb05aafb88"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-754-03)", "package_ndc": "65162-754-03", "marketing_start_date": "20100202"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-754-10)", "package_ndc": "65162-754-10", "marketing_start_date": "20100202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-754-50)", "package_ndc": "65162-754-50", "marketing_start_date": "20100202"}], "brand_name": "Benazepril Hydrochloride", "product_id": "65162-754_1897ce48-56e1-415f-9db3-224c48b3063e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "65162-754", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20100202", "listing_expiration_date": "20261231"}