PredniSONE Tablets, USP, 20 mg

NDC 63561-0122 · Granulation Technology, Inc.

Generic namePredniSONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

63561-0122-1 — 100 TABLET in 1 BOTTLE (63561-0122-1)

63561-0122-2 — 1000 TABLET in 1 BOTTLE (63561-0122-2)

63561-0122-5 — 500 TABLET in 1 BOTTLE (63561-0122-5)

FDA lists these products with the same active ingredient.

62135-553 — Prednisone, 63187-020 — Prednisone, 63187-037 — Prednisone, 63187-066 — Prednisone, 63187-243 — PredniSONE, 63187-300 — Prednisone, 63187-807 — Prednisone, 63187-997 — Prednisone, 63561-0120 — PredniSONE, 63561-0121 — PredniSONE, 63629-1605 — Prednisone, 63629-2254 — Prednisone, 63629-2257 — Prednisone, 63629-2260 — Prednisone, 63629-2264 — Prednisone, 64380-782 — PREDNISONE, 64380-783 — PREDNISONE, 64380-784 — PREDNISONE, 64380-785 — PREDNISONE, 64380-835 — 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.