Package 68071-3324-3

{"route": ["ORAL"], "spl_id": "1cd70bab-30c9-fbdd-e063-6294a90a7df3", "openfda": {"upc": ["0368071332438"], "unii": ["N1SN99T69T"], "rxcui": ["898723"], "spl_set_id": ["53fea330-cc4a-3b7e-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (68071-3324-1)", "package_ndc": "68071-3324-1", "marketing_start_date": "20170710"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68071-3324-3)", "package_ndc": "68071-3324-3", "marketing_start_date": "20170710"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68071-3324-6)", "package_ndc": "68071-3324-6", "marketing_start_date": "20170710"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68071-3324_1cd70bab-30c9-fbdd-e063-6294a90a7df3", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-3324", "generic_name": "Benazepril Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}