Prednisone

NDC 42708-105 · QPharma, Inc.

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

42708-105-10 — 10 TABLET in 1 BOTTLE (42708-105-10)

FDA lists these products with the same active ingredient.

0615-8440 — prednisone, 0615-8441 — prednisone, 0904-6923 — Prednisone, 10135-775 — Prednisone, 10135-776 — Prednisone, 10135-777 — Prednisone, 10135-778 — Prednisone, 10135-779 — Prednisone, 17856-3722 — PredniSONE, 42708-045 — PredniSONE, 42708-114 — Prednisone, 42708-115 — Prednisone, 42708-136 — Prednisone, 42708-166 — PREDNISONE, 42708-186 — PREDNISONE, 42708-195 — PREDNISONE, 43063-968 — PredniSONE, 43598-886 — Prednisone, 43598-887 — Prednisone, 43598-888 — 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.