prednisone

NDC 70518-4354 · REMEDYREPACK INC.

Generic nameprednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength10 mg/1

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

Marketing categoryANDA

Packages

70518-4354-0 — 30 TABLET in 1 BLISTER PACK (70518-4354-0)

FDA lists these products with the same active ingredient.

70518-3476 — PREDNISONE, 70518-3537 — Prednisone, 70518-3539 — PREDNISONE, 70518-3540 — prednisone, 70518-3555 — PREDNISONE, 70518-4038 — PREDNISONE, 70518-4191 — PredniSONE, 70518-4243 — PREDNISONE, 70518-4271 — PredniSONE, 70518-4293 — PREDNISONE, 70518-4560 — PREDNISONE, 70518-4660 — PREDNISONE, 70954-056 — Prednisone, 70954-057 — Prednisone, 70954-058 — Prednisone, 70954-059 — Prednisone, 70954-060 — Prednisone, 70954-061 — Prednisone, 71205-089 — Prednisone, 71205-239 — 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.