PredniSONE

NDC 51655-701 · Northwind Health Company, LLC

Generic namePredniSONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

51655-701-18 — 18 TABLET in 1 BOTTLE, PLASTIC (51655-701-18)

51655-701-20 — 20 TABLET in 1 BOTTLE, PLASTIC (51655-701-20)

51655-701-53 — 10 TABLET in 1 BOTTLE, PLASTIC (51655-701-53)

FDA lists these products with the same active ingredient.

51407-923 — Prednisone, 51655-068 — PREDNISONE, 51655-197 — Prednisone, 51655-242 — Prednisone, 51655-349 — PREDNISONE, 51655-355 — PredniSONE, 51655-359 — Prednisone, 51655-410 — Prednisone, 51655-493 — PredniSONE, 51655-541 — PREDNISONE, 51655-726 — PredniSONE, 51655-763 — PredniSONE, 51655-765 — Prednisone, 51655-935 — Prednisone, 51655-939 — PredniSONE, 51655-972 — PREDNISONE, 51655-988 — prednisone, 54348-506 — PREDNISONE, 55154-2146 — Prednisone, 55154-2147 — 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.