PREDNISONE

NDC 59651-484 · Aurobindo Pharma Limited

Generic namePREDNISONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength1 mg/1

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

Marketing categoryANDA

Packages

59651-484-01 — 100 TABLET in 1 BOTTLE (59651-484-01)

59651-484-78 — 10 BLISTER PACK in 1 CARTON (59651-484-78) / 10 TABLET in 1 BLISTER PACK

59651-484-99 — 1000 TABLET in 1 BOTTLE (59651-484-99)

FDA lists these products with the same active ingredient.

51655-939 — PredniSONE, 51655-972 — PREDNISONE, 51655-988 — prednisone, 54348-506 — PREDNISONE, 55154-2146 — Prednisone, 55154-2147 — Prednisone, 55154-2581 — Prednisone, 55154-2582 — PREDNISONE, 55154-3564 — Prednisone, 55289-330 — PredniSONE, 59651-485 — PREDNISONE, 59651-486 — PREDNISONE, 59651-487 — PREDNISONE, 59651-488 — PREDNISONE, 59651-489 — PREDNISONE, 60219-1705 — prednisone, 60219-1706 — prednisone, 60219-1707 — prednisone, 60219-1708 — prednisone, 60687-122 — 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.