Prednisone D/P

NDC 72189-646 · Direct_Rx

Generic namePrednisone D/P

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength10 mg/1

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

Marketing categoryANDA

Packages

72189-646-21 — 21 TABLET in 1 CARTON (72189-646-21)

FDA lists these products with the same active ingredient.

71610-834 — Prednisone, 72162-1169 — Prednisone, 72162-2149 — Prednisone, 72162-2484 — PredniSONE, 72162-2485 — PredniSONE, 72162-2486 — PredniSONE, 72189-430 — Prednisone, 72189-489 — Prednisone, 72189-589 — Prednisone, 72189-593 — Prednisone, 72189-673 — Prednisone D/P, 72789-393 — Prednisone, 72789-401 — Prednisone, 72789-413 — Prednisone, 72789-426 — PREDNISONE, 72789-448 — Prednisone, 72789-473 — PredniSONE, 72789-474 — PredniSONE, 72789-475 — PredniSONE, 72789-498 — 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.