Package 71335-2185-2

{"route": ["ORAL"], "spl_id": "380d3ff6-47d7-4cc3-8889-8fe07f78f894", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["f6f688d0-cb13-40af-a65f-480c37334e37"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2185-1)", "package_ndc": "71335-2185-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2185-2)", "package_ndc": "71335-2185-2", "marketing_start_date": "20240403"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2185-3)", "package_ndc": "71335-2185-3", "marketing_start_date": "20230124"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2185-4)", "package_ndc": "71335-2185-4", "marketing_start_date": "20221129"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2185-5)", "package_ndc": "71335-2185-5", "marketing_start_date": "20240403"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "71335-2185_380d3ff6-47d7-4cc3-8889-8fe07f78f894", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71335-2185", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040604", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}