Package 68788-6957-6

{"route": ["ORAL"], "spl_id": "5149af12-5ae1-458d-835d-915134a40e2b", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["4d5a8b50-dd2f-4329-9e28-93608e8fe8da"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (68788-6957-1)", "package_ndc": "68788-6957-1", "marketing_start_date": "20170502"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68788-6957-3)", "package_ndc": "68788-6957-3", "marketing_start_date": "20170502"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68788-6957-6)", "package_ndc": "68788-6957-6", "marketing_start_date": "20170502"}, {"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (68788-6957-8)", "package_ndc": "68788-6957-8", "marketing_start_date": "20170502"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68788-6957-9)", "package_ndc": "68788-6957-9", "marketing_start_date": "20170502"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68788-6957_5149af12-5ae1-458d-835d-915134a40e2b", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68788-6957", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20170502", "listing_expiration_date": "20261231"}