Package 0088-2161-30

{"route": ["ORAL"], "spl_id": "765327c7-cb5b-4637-84da-4fd9a024ad96", "openfda": {"nui": ["N0000175713"], "unii": ["G162GK9U4W"], "rxcui": ["205284", "205285", "205286", "213377", "213379", "213380"], "spl_set_id": ["320f63f2-fac3-4aee-aff8-85724e00ef52"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["sanofi-aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0088-2161-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0088-2161-30", "marketing_start_date": "19980919"}], "brand_name": "Arava", "product_id": "0088-2161_765327c7-cb5b-4637-84da-4fd9a024ad96", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "0088-2161", "generic_name": "leflunomide", "labeler_name": "sanofi-aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Arava", "active_ingredients": [{"name": "LEFLUNOMIDE", "strength": "20 mg/1"}], "application_number": "NDA020905", "marketing_category": "NDA", "marketing_start_date": "19980910", "listing_expiration_date": "20261231"}