Package 50090-3775-0

{"route": ["ORAL"], "spl_id": "47e4a35d-5bf0-4098-a64b-345b5a87e454", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["6c24bb4c-42d2-483a-b33f-95182b32b93d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50090-3775-0)", "package_ndc": "50090-3775-0", "marketing_start_date": "20181105"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (50090-3775-2)", "package_ndc": "50090-3775-2", "marketing_start_date": "20181105"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50090-3775_47e4a35d-5bf0-4098-a64b-345b5a87e454", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-3775", "generic_name": "Benazepril Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}