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Hydrocortisone

NDC 71741-455 · Redmont Pharmaceuticals, LLC

Generic namehydrocortisone
Dosage formGEL
RouteTOPICAL
Active ingredient(s)HYDROCORTISONE
Strength20 mg/g
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryUNAPPROVED DRUG OTHER

Packages

71741-455-31 — 30 g in 1 TUBE (71741-455-31)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71297-010 — Hydrocortisone Lotion, 71335-1989 — hydrocortisone, 71335-2044 — hydrocortisone, 71335-2770 — HYDROCORTISONE, 71335-2918 — hydrocortisone, 71335-2954 — Hydrocortisone, 71399-0120 — Hydrocortisone, 71399-0180 — Hydrocortisone, 71516-342 — HYDROCORTISONE, 71656-064 — hydrocortisone and acetic acid otic, 71863-109 — Hydrocortisone, 71863-110 — Hydrocortisone, 71863-111 — Hydrocortisone, 71863-112 — Hydrocortisone, 71863-116 — Hydrocortisone, 71930-078 — hydrocortisone, 71930-079 — hydrocortisone, 71930-080 — hydrocortisone, 72162-1382 — Hydrocortisone, 72162-1383 — Hydrocortisone, +498 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels