Package 50090-3243-0

{"route": ["ORAL"], "spl_id": "fdee60ff-213d-4b76-8c7b-952cbb037ad9", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["7aac6a2f-85fb-4c7a-b424-9c253186dffe"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50090-3243-0)", "package_ndc": "50090-3243-0", "marketing_start_date": "20171117"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-3243-1)", "package_ndc": "50090-3243-1", "marketing_start_date": "20171103"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50090-3243_fdee60ff-213d-4b76-8c7b-952cbb037ad9", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-3243", "generic_name": "Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20271231"}