Package 68788-8877-6

{"route": ["ORAL"], "spl_id": "91a3d0f7-d2df-4230-ad9e-b32f7312d337", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["91a3d0f7-d2df-4230-ad9e-b32f7312d337"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1)", "package_ndc": "68788-8877-1", "marketing_start_date": "20250519"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3)", "package_ndc": "68788-8877-3", "marketing_start_date": "20250519"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6)", "package_ndc": "68788-8877-6", "marketing_start_date": "20250519"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)", "package_ndc": "68788-8877-9", "marketing_start_date": "20250519"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68788-8877_91a3d0f7-d2df-4230-ad9e-b32f7312d337", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68788-8877", "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": "10 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20250519", "listing_expiration_date": "20261231"}