Prednisone delayed release

NDC 43598-888 · Dr. Reddys Laboratories Inc.

Generic namePrednisone

Dosage formTABLET, DELAYED RELEASE

RouteORAL

Active ingredient(s)PREDNISONE

Strength5 mg/1

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

Marketing categoryANDA

Packages

43598-888-01 — 1 BOTTLE in 1 CARTON (43598-888-01) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE

43598-888-30 — 1 BOTTLE in 1 CARTON (43598-888-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE

FDA lists these products with the same active ingredient.

42708-105 — Prednisone, 42708-114 — Prednisone, 42708-115 — Prednisone, 42708-136 — Prednisone, 42708-166 — PREDNISONE, 42708-186 — PREDNISONE, 42708-195 — PREDNISONE, 43063-968 — PredniSONE, 43598-886 — Prednisone, 43598-887 — Prednisone, 45865-884 — PREDNISONE, 50090-0439 — Prednisone, 50090-1001 — Prednisone, 50090-1002 — Prednisone, 50090-2786 — Prednisone, 50090-2789 — Prednisone, 50090-2804 — Prednisone, 50090-3137 — Prednisone, 50090-3354 — Prednisone, 50090-3361 — Prednisone, +288 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.