PredniSONE Tablets, USP, 20 mg

NDC 71335-2754 · Bryant Ranch Prepack

Generic namePredniSONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

71335-2754-0 11 TABLET in 1 BOTTLE (71335-2754-0)

71335-2754-1 20 TABLET in 1 BOTTLE (71335-2754-1)

71335-2754-2 30 TABLET in 1 BOTTLE (71335-2754-2)

71335-2754-3 40 TABLET in 1 BOTTLE (71335-2754-3)

71335-2754-4 15 TABLET in 1 BOTTLE (71335-2754-4)

71335-2754-5 10 TABLET in 1 BOTTLE (71335-2754-5)

71335-2754-6 21 TABLET in 1 BOTTLE (71335-2754-6)

71335-2754-7 18 TABLET in 1 BOTTLE (71335-2754-7)

71335-2754-8 12 TABLET in 1 BOTTLE (71335-2754-8)

71335-2754-9 23 TABLET in 1 BOTTLE (71335-2754-9)

FDA lists these products with the same active ingredient.

71335-2134 — PREDNISONE, 71335-2149 — PREDNISONE, 71335-2160 — Prednisone, 71335-2273 — PREDNISONE, 71335-2356 — PREDNISONE, 71335-2389 — PREDNISONE, 71335-2736 — PredniSONE, 71335-2737 — PredniSONE, 71335-2752 — PredniSONE, 71335-2753 — PredniSONE, 71335-2895 — PREDNISONE, 71335-2938 — PredniSONE, 71335-3042 — PredniSONE, 71335-3043 — PredniSONE, 71335-3044 — PredniSONE, 71335-3045 — PredniSONE, 71335-3046 — PredniSONE, 71335-3047 — PredniSONE, 71335-3129 — Prednisone, 71335-9715 — 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.