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Prednisone

NDC 70954-059 · ANI Pharmaceuticals, Inc.

Generic namePrednisone
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength10 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

70954-059-10 — 100 TABLET in 1 BOTTLE (70954-059-10)

70954-059-20 — 1000 TABLET in 1 BOTTLE (70954-059-20)

70954-059-30 — 1 BLISTER PACK in 1 BOX (70954-059-30) / 21 TABLET in 1 BLISTER PACK

70954-059-40 — 1 BLISTER PACK in 1 BOX (70954-059-40) / 48 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4191 — PredniSONE, 70518-4243 — PREDNISONE, 70518-4271 — PredniSONE, 70518-4293 — PREDNISONE, 70518-4354 — prednisone, 70518-4560 — PREDNISONE, 70518-4660 — PREDNISONE, 70954-056 — Prednisone, 70954-057 — Prednisone, 70954-058 — Prednisone, 70954-060 — Prednisone, 70954-061 — 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, +288 more

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