Package 0054-0400-22

{"route": ["ORAL"], "spl_id": "c5148154-683f-4369-bb65-9f6f43a64e2b", "openfda": {"upc": ["0300540400132", "0300540603137"], "unii": ["ZB22ENF0XR"], "rxcui": ["1607617", "1874553", "1874559"], "spl_set_id": ["662890ff-d254-40e0-a9fe-f07ab94d65d6"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0054-0400-13)", "package_ndc": "0054-0400-13", "marketing_start_date": "20170301"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0054-0400-22)", "package_ndc": "0054-0400-22", "marketing_start_date": "20170301"}], "brand_name": "Desvenlafaxine", "product_id": "0054-0400_c5148154-683f-4369-bb65-9f6f43a64e2b", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0054-0400", "generic_name": "Desvenlafaxine", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA204083", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}