Prednisone

NDC 70954-061 · ANI Pharmaceuticals, Inc.

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength50 mg/1

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

Marketing categoryANDA

Packages

70954-061-10 — 100 TABLET in 1 BOTTLE (70954-061-10)

FDA lists these products with the same active ingredient.

70518-4271 — PredniSONE, 70518-4293 — PREDNISONE, 70518-4354 — prednisone, 70518-4560 — PREDNISONE, 70518-4660 — PREDNISONE, 70954-056 — Prednisone, 70954-057 — Prednisone, 70954-058 — Prednisone, 70954-059 — Prednisone, 70954-060 — Prednisone, 71205-089 — Prednisone, 71205-239 — Prednisone, 71205-362 — Prednisone, 71205-407 — Prednisone, 71205-421 — Prednisone, 71205-665 — Prednisone, 71205-729 — PREDNISONE, 71205-741 — PREDNISONE, 71205-755 — PREDNISONE, 71205-797 — 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.