PredniSONE Tablets, USP, 20 mg

NDC 72789-500 · PD-Rx Pharmaceuticals, Inc.

Generic namePredniSONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

72789-500-21 — 21 TABLET in 1 BOTTLE, PLASTIC (72789-500-21)

J7512 — Prednisone, immediate release or delayed release, oral, 1 mg Medicare Part B payment limit (ASP + 6%): $0.00

FDA lists these products with the same active ingredient.

72189-673 — Prednisone D/P, 72789-393 — Prednisone, 72789-401 — Prednisone, 72789-413 — Prednisone, 72789-426 — PREDNISONE, 72789-448 — Prednisone, 72789-473 — PredniSONE, 72789-474 — PredniSONE, 72789-475 — PredniSONE, 72789-498 — PredniSONE, 72789-509 — PredniSONE, 72789-513 — PredniSONE, 74157-010 — Prednisone, 74157-019 — Prednisone, 76420-067 — Prednisone, 76420-068 — Prednisone, 76420-069 — Prednisone, 76420-412 — PREDNISONE, 76420-413 — PREDNISONE, 76420-414 — 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.