Prednisone

NDC 68788-9551 · Preferred Pharmaceuticals, Inc.

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength5 mg/1

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

Marketing categoryANDA

Packages

68788-9551-2 — 21 TABLET in 1 BOX, UNIT-DOSE (68788-9551-2)

FDA lists these products with the same active ingredient.

68071-3821 — Prednisone, 68071-3958 — PREDNISONE, 68071-4685 — Prednisone, 68788-8166 — PREDNISONE, 68788-8184 — PREDNISONE, 68788-8579 — PREDNISONE, 68788-8663 — PREDNISONE, 68788-8819 — PREDNISONE, 68788-8858 — PREDNISONE, 68788-8898 — PREDNISONE, 70518-0305 — Prednisone, 70518-3401 — PREDNISONE, 70518-3476 — PREDNISONE, 70518-3537 — Prednisone, 70518-3539 — PREDNISONE, 70518-3540 — prednisone, 70518-3555 — PREDNISONE, 70518-4038 — PREDNISONE, 70518-4191 — PredniSONE, 70518-4243 — PREDNISONE, +288 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.