Prednisone

NDC 76420-069 · Asclemed USA, Inc.

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

76420-069-10 — 10 TABLET in 1 BOTTLE (76420-069-10)

76420-069-15 — 15 TABLET in 1 BOTTLE (76420-069-15)

76420-069-20 — 20 TABLET in 1 BOTTLE (76420-069-20)

76420-069-21 — 21 TABLET in 1 BOTTLE (76420-069-21)

76420-069-30 — 30 TABLET in 1 BOTTLE (76420-069-30)

FDA lists these products with the same active ingredient.

72789-474 — PredniSONE, 72789-475 — PredniSONE, 72789-498 — PredniSONE, 72789-500 — PredniSONE, 72789-509 — PredniSONE, 72789-513 — PredniSONE, 74157-010 — Prednisone, 74157-019 — Prednisone, 76420-067 — Prednisone, 76420-068 — Prednisone, 76420-412 — PREDNISONE, 76420-413 — PREDNISONE, 76420-414 — PREDNISONE, 80425-0068 — Prednisone, 80425-0069 — Prednisone, 80425-0105 — Prednisone, 80425-0106 — Prednisone, 80425-0193 — Prednisone, 80425-0479 — PREDNISONE, 80425-0480 — 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.