Package 0168-0056-15

{"route": ["TOPICAL"], "spl_id": "b3e9355b-1499-4430-9cdd-8ba0f77279c4", "openfda": {"upc": ["0301680055466", "0301680056159"], "unii": ["826Y60901U"], "rxcui": ["197405", "238920", "240209"], "spl_set_id": ["97dde5f5-a865-4af2-b562-8da72c8475f3"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0168-0056-15)  / 15 g in 1 TUBE", "package_ndc": "0168-0056-15", "marketing_start_date": "19840904"}, {"sample": false, "description": "1 TUBE in 1 CARTON (0168-0056-46)  / 45 g in 1 TUBE", "package_ndc": "0168-0056-46", "marketing_start_date": "19840904"}], "brand_name": "Betamethasone Dipropionate", "product_id": "0168-0056_b3e9355b-1499-4430-9cdd-8ba0f77279c4", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0056", "generic_name": "Betamethasone Dipropionate", "labeler_name": "E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "NDA019141", "marketing_category": "NDA", "marketing_start_date": "19840904", "listing_expiration_date": "20271231"}