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Hydrocortisone

NDC 51672-3003 · Sun Pharmaceutical Industries, Inc.

Generic nameHydrocortisone
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)HYDROCORTISONE
Strength25 mg/g
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

51672-3003-0 — 1 TUBE in 1 CARTON (51672-3003-0) / 20 g in 1 TUBE

51672-3003-2 — 1 TUBE in 1 CARTON (51672-3003-2) / 28.35 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-165 — Hydrocortisone Ointment, 51316-227 — HYDROCORTISONE, 51316-230 — HYDROCORTISONE, 51316-388 — Hydrocortisone, 51326-108 — Hydrocortisone, 51628-4527 — Hydrocortisone 1.0%(w/w), 51672-2010 — Hydrocortisone, 51672-2013 — Hydrocortisone, 51672-2018 — Hydrocortisone, 51672-2063 — Hydrocortisone, 51672-3007 — Hydrocortisone and Acetic Acid, 51672-5330 — Hydrocortisone Cream 1%, 51822-021 — HYDROCORTISONE, 51824-097 — Hydrocortisone, 51824-098 — Hydrocortisone, 51824-114 — Hydrocortisone, 51824-197 — Hydrocortisone, 52000-022 — Hydrocortisone, 52187-532 — hydrocortisone, iodoquinol, 53329-091 — hydrocortisone, +498 more

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