Prednisone

NDC 10135-778 · Marlex Pharmaceuticals, Inc.

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

Marketing categoryANDA

Packages

10135-778-01 — 100 TABLET in 1 BOTTLE (10135-778-01)

10135-778-05 — 500 TABLET in 1 BOTTLE (10135-778-05)

10135-778-10 — 1000 TABLET in 1 BOTTLE (10135-778-10)

FDA lists these products with the same active ingredient.

0603-5338 — Prednisone, 0603-5339 — Prednisone, 0615-8438 — PREDNISONE, 0615-8439 — prednisone, 0615-8440 — prednisone, 0615-8441 — prednisone, 0904-6923 — Prednisone, 10135-775 — Prednisone, 10135-776 — Prednisone, 10135-777 — Prednisone, 10135-779 — Prednisone, 17856-3722 — PredniSONE, 42708-045 — PredniSONE, 42708-105 — Prednisone, 42708-114 — Prednisone, 42708-115 — Prednisone, 42708-136 — Prednisone, 42708-166 — PREDNISONE, 42708-186 — PREDNISONE, 42708-195 — PREDNISONE, +288 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.