Package 59651-499-05

{"route": ["ORAL"], "spl_id": "9de2de56-614f-4294-8794-d30758cf5f70", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["9de2de56-614f-4294-8794-d30758cf5f70"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-499-01)", "package_ndc": "59651-499-01", "marketing_start_date": "20211007"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59651-499-05)", "package_ndc": "59651-499-05", "marketing_start_date": "20211007"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (59651-499-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "59651-499-78", "marketing_start_date": "20211007"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (59651-499-99)", "package_ndc": "59651-499-99", "marketing_start_date": "20211007"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "59651-499_9de2de56-614f-4294-8794-d30758cf5f70", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "59651-499", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA087871", "marketing_category": "ANDA", "marketing_start_date": "20211007", "listing_expiration_date": "20261231"}