PREDNISONE

NDC 42708-195 · 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

42708-195-10 — 10 TABLET in 1 BOTTLE, PLASTIC (42708-195-10)

FDA lists these products with the same active ingredient.

10135-778 — 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, 43063-968 — PredniSONE, 43598-886 — Prednisone, 43598-887 — Prednisone, 43598-888 — Prednisone, 45865-884 — PREDNISONE, 50090-0439 — Prednisone, 50090-1001 — Prednisone, 50090-1002 — Prednisone, 50090-2786 — Prednisone, 50090-2789 — Prednisone, +288 more

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