Prednisone

NDC 51655-197 · Northwind Health Company, LLC

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength2.5 mg/1

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

Marketing categoryANDA

Packages

51655-197-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-197-52)

FDA lists these products with the same active ingredient.

50090-7686 — prednisone, 50090-7688 — prednisone, 50090-7825 — PREDNISONE, 50090-7931 — PREDNISONE, 50090-7933 — PREDNISONE, 50090-7935 — PREDNISONE, 51407-921 — Prednisone, 51407-922 — Prednisone, 51407-923 — Prednisone, 51655-068 — PREDNISONE, 51655-242 — Prednisone, 51655-349 — PREDNISONE, 51655-355 — PredniSONE, 51655-359 — Prednisone, 51655-410 — Prednisone, 51655-493 — PredniSONE, 51655-541 — PREDNISONE, 51655-701 — PredniSONE, 51655-726 — PredniSONE, 51655-763 — 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.