Prednisone

NDC 72189-589 · Direct_Rx

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength10 mg/1

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

Marketing categoryANDA

Packages

72189-589-10 — 10 TABLET in 1 BOTTLE (72189-589-10)

72189-589-15 — 15 TABLET in 1 BOTTLE (72189-589-15)

72189-589-21 — 21 TABLET in 1 BOTTLE (72189-589-21)

72189-589-30 — 30 TABLET in 1 BOTTLE (72189-589-30)

FDA lists these products with the same active ingredient.

71335-3129 — Prednisone, 71335-9715 — PREDNISONE, 71610-834 — Prednisone, 72162-1169 — Prednisone, 72162-2149 — Prednisone, 72162-2484 — PredniSONE, 72162-2485 — PredniSONE, 72162-2486 — PredniSONE, 72189-430 — Prednisone, 72189-489 — Prednisone, 72189-593 — Prednisone, 72189-646 — Prednisone D/P, 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, +288 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.