Prednisone

NDC 50090-2804 · A-S Medication Solutions

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

50090-2804-0 — 20 TABLET in 1 BOTTLE (50090-2804-0)

50090-2804-2 — 6 TABLET in 1 BOTTLE (50090-2804-2)

50090-2804-5 — 14 TABLET in 1 BOTTLE (50090-2804-5)

50090-2804-7 — 15 TABLET in 1 BOTTLE (50090-2804-7)

FDA lists these products with the same active ingredient.

43063-968 — PredniSONE, 43598-886 — Prednisone, 43598-887 — Prednisone, 43598-888 — Prednisone, 45865-884 — PREDNISONE, 50090-0439 — Prednisone, 50090-1001 — Prednisone, 50090-1002 — Prednisone, 50090-2786 — Prednisone, 50090-2789 — Prednisone, 50090-3137 — Prednisone, 50090-3354 — Prednisone, 50090-3361 — Prednisone, 50090-5202 — Prednisone, 50090-5814 — PREDNISONE, 50090-6122 — prednisone, 50090-6123 — prednisone, 50090-6225 — Prednisone, 50090-6259 — prednisone, 50090-6376 — 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.