Package 54766-763-04

Brand: pramosone

Generic: hydrocortisone acetate and pramoxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 54766-763-04
Digits Only 5476676304
Product NDC 54766-763
Product ID 54766-763_26a40470-e73f-8fb9-e063-6294a90aa179
Description

28.4 g in 1 TUBE (54766-763-04)

Marketing

Marketing Status
Discontinued 2026-03-31
Brand pramosone
Generic hydrocortisone acetate and pramoxine hydrochloride
Sample Package No

Linked Drug Pages (1)

pramosone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "26a40470-e73f-8fb9-e063-6294a90aa179", "openfda": {"unii": ["3X7931PO74", "88AYB867L5"], "rxcui": ["1234317", "1234322"], "spl_set_id": ["d4d85400-3bb3-11e5-830e-0002a5d5c51b"], "manufacturer_name": ["Sebela Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28.4 g in 1 TUBE (54766-763-04)", "package_ndc": "54766-763-04", "marketing_end_date": "20260331", "marketing_start_date": "20150805"}], "brand_name": "pramosone", "product_id": "54766-763_26a40470-e73f-8fb9-e063-6294a90aa179", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "54766-763", "generic_name": "hydrocortisone acetate and pramoxine hydrochloride", "labeler_name": "Sebela Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pramosone", "active_ingredients": [{"name": "HYDROCORTISONE ACETATE", "strength": "10 mg/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_end_date": "20260331", "marketing_start_date": "20150805"}