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PREDNISONE

NDC 70518-4243 · REMEDYREPACK INC.

Generic namePREDNISONE
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength20 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

70518-4243-0 — 30 TABLET in 1 BLISTER PACK (70518-4243-0)

70518-4243-1 — 10 TABLET in 1 BOTTLE, PLASTIC (70518-4243-1)

70518-4243-2 — 14 TABLET in 1 BOTTLE, PLASTIC (70518-4243-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-9551 — 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, 70518-4271 — 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, +288 more

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