Package 68071-1969-3

{"route": ["ORAL"], "spl_id": "1d605356-58f1-2e0a-e063-6294a90af384", "openfda": {"upc": ["0368071196993"], "unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["700c828c-86c6-1857-e053-2a91aa0ae314"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (68071-1969-2)", "package_ndc": "68071-1969-2", "marketing_start_date": "20180702"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68071-1969-3)", "package_ndc": "68071-1969-3", "marketing_start_date": "20180702"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68071-1969-6)", "package_ndc": "68071-1969-6", "marketing_start_date": "20180702"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68071-1969-9)", "package_ndc": "68071-1969-9", "marketing_start_date": "20180702"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68071-1969_1d605356-58f1-2e0a-e063-6294a90af384", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-1969", "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": "20 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}