Package 68788-9313-9

{"route": ["ORAL"], "spl_id": "dede72c0-6cd9-4415-96f8-79693fc25126", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687", "898690"], "spl_set_id": ["032ea0f7-3304-4778-b3a6-6125ea7537ab"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (68788-9313-1)", "package_ndc": "68788-9313-1", "marketing_start_date": "20150325"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68788-9313-3)", "package_ndc": "68788-9313-3", "marketing_start_date": "20150325"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68788-9313-6)", "package_ndc": "68788-9313-6", "marketing_start_date": "20150325"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (68788-9313-9)", "package_ndc": "68788-9313-9", "marketing_start_date": "20150325"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68788-9313_dede72c0-6cd9-4415-96f8-79693fc25126", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68788-9313", "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": "20 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20150325", "listing_expiration_date": "20261231"}