Package 16571-115-10

{"route": ["ORAL"], "spl_id": "20aba551-c0c0-4ea1-8200-ad81956ff294", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["6a1a48ac-8ad5-4363-b298-d9825ae2a448"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16571-115-01)", "package_ndc": "16571-115-01", "marketing_start_date": "20230822"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16571-115-10)", "package_ndc": "16571-115-10", "marketing_start_date": "20230822"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16571-115-50)", "package_ndc": "16571-115-50", "marketing_start_date": "20230822"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "16571-115_20aba551-c0c0-4ea1-8200-ad81956ff294", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "16571-115", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20230822", "listing_expiration_date": "20261231"}