Package 31722-044-12

{"route": ["ORAL"], "spl_id": "eaf892a4-41c4-70e0-e053-2995a90a2079", "openfda": {"nui": ["N0000175956", "N0000175955", "N0000008683"], "upc": ["0331722044127"], "unii": ["V1L22WVE2S"], "rxcui": ["730834"], "spl_set_id": ["94313e24-9534-4b6c-b374-c436c4916303"], "pharm_class_pe": ["Decreased Leukotriene Production [PE]"], "pharm_class_epc": ["5-Lipoxygenase Inhibitor [EPC]"], "pharm_class_moa": ["5-Lipoxygenase Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-044-12)", "package_ndc": "31722-044-12", "marketing_start_date": "20221011"}], "brand_name": "Zileuton", "product_id": "31722-044_eaf892a4-41c4-70e0-e053-2995a90a2079", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["5-Lipoxygenase Inhibitor [EPC]", "5-Lipoxygenase Inhibitors [MoA]", "Decreased Leukotriene Production [PE]"], "product_ndc": "31722-044", "generic_name": "Zileuton", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zileuton", "active_ingredients": [{"name": "ZILEUTON", "strength": "600 mg/1"}], "application_number": "ANDA215742", "marketing_category": "ANDA", "marketing_start_date": "20221011", "listing_expiration_date": "20261231"}