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Hydrocortisone

NDC 72789-229 · PD-Rx Pharmaceuticals, Inc.

Generic nameHydrocortisone
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCORTISONE
Strength20 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

72789-229-01 — 100 TABLET in 1 BOTTLE, PLASTIC (72789-229-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-2284 — hydrocortisone, 72189-209 — HYDROCORTISONE, 72189-554 — Hydrocortisone Cream, 72189-625 — Hydrocortisone Cream, 72288-369 — Hydrocortisone, 72288-713 — Hydrocortisone, 72288-878 — Hydrocortisone, 72288-973 — hydrocortisone, 72789-227 — Hydrocortisone, 72789-228 — Hydrocortisone, 72839-113 — Hydrocortisone 1%, 73141-622 — hydrocortisone, 73352-455 — Hydrocortisone, 73408-933 — Hydrocortisone, 73408-937 — Hydrocortisone, 73492-291 — 1% Hydrocortisone Anti-itch, 75742-070 — Hydrocortisone 1.0%(w/w), 76314-002 — HYDROCORTISONE, 76314-003 — HYDROCORTISONE, 76314-004 — 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