Package 68788-7845-1

{"route": ["ORAL"], "spl_id": "4ae04e1d-305d-438a-86b4-b474b1e891e1", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["6d24bcc1-e5f4-4d65-9858-5fc583efe572"], "manufacturer_name": ["Preferred Pharmaceuticlas Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7845-1)", "package_ndc": "68788-7845-1", "marketing_start_date": "20210120"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7845-3)", "package_ndc": "68788-7845-3", "marketing_start_date": "20210120"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7845-6)", "package_ndc": "68788-7845-6", "marketing_start_date": "20210120"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-7845-8)", "package_ndc": "68788-7845-8", "marketing_start_date": "20210120"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7845-9)", "package_ndc": "68788-7845-9", "marketing_start_date": "20210120"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68788-7845_4ae04e1d-305d-438a-86b4-b474b1e891e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68788-7845", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Preferred Pharmaceuticlas Inc.", "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": "20210120", "listing_expiration_date": "20261231"}