PredniSONE

NDC 0054-8740 · Hikma Pharmaceuticals USA Inc.

Generic namePredniSONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength2.5 mg/1

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

Marketing categoryANDA

Packages

0054-8740-25 — 10 BLISTER PACK in 1 CARTON (0054-8740-25) / 10 TABLET in 1 BLISTER PACK

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.

0054-0017 — PredniSONE, 0054-0018 — PredniSONE, 0054-0019 — PredniSONE, 0054-3721 — PredniSONE Intensol, 0054-3722 — PredniSONE, 0054-4728 — PredniSONE, 0054-4741 — PredniSONE, 0054-4742 — PredniSONE, 0054-8724 — PredniSONE, 0054-8739 — PredniSONE, 0054-9817 — PredniSONE, 0054-9818 — PredniSONE, 0054-9828 — PredniSONE, 0378-0640 — Prednisone, 0378-0641 — Prednisone, 0378-0642 — Prednisone, 0591-5052 — Prednisone, 0591-5442 — Prednisone, 0591-5443 — Prednisone, 0603-5335 — 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.