Prednisone

NDC 42708-114 · QPharma, Inc.

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength5 mg/1

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

Marketing categoryANDA

Packages

42708-114-21 — 21 TABLET in 1 BOTTLE (42708-114-21)

FDA lists these products with the same active ingredient.

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, 42708-105 — 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, 45865-884 — 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.