Package 75834-197-01

{"route": ["TOPICAL"], "spl_id": "53ac723b-1f67-47e5-b560-6589342a27d8", "openfda": {"upc": ["0375834197012"], "unii": ["3X7931PO74", "88AYB867L5"], "rxcui": ["1294025"], "spl_set_id": ["dc7f17e4-76f8-4cd4-a7e3-43032b386b74"], "manufacturer_name": ["Nivagen Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (75834-197-01)  / 28.5 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "75834-197-01", "marketing_start_date": "20190429"}], "brand_name": "HYDROCORTISONE ACETATE PRAMOXINE HYDROCHLORIDE", "product_id": "75834-197_53ac723b-1f67-47e5-b560-6589342a27d8", "dosage_form": "CREAM", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "75834-197", "generic_name": "PRAMOXINE HYDROCHLORIDE and HYDROCORTISONE ACETATE", "labeler_name": "Nivagen Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCORTISONE ACETATE PRAMOXINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROCORTISONE ACETATE", "strength": "25 mg/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20190429", "listing_expiration_date": "20261231"}