prednisone

NDC 60760-790 · St. Mary's Medical Park Pharmacy

Generic namePREDNISONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

60760-790-12 — 12 TABLET in 1 BOTTLE, PLASTIC (60760-790-12)

60760-790-21 — 21 TABLET in 1 BOTTLE, PLASTIC (60760-790-21)

FDA lists these products with the same active ingredient.

60219-1706 — prednisone, 60219-1707 — prednisone, 60219-1708 — prednisone, 60687-122 — Prednisone, 60687-134 — Prednisone, 60687-145 — Prednisone, 60687-854 — Prednisone, 60687-903 — PREDNISONE, 60687-914 — Prednisone, 60687-925 — Prednisone, 60760-796 — PredniSONE, 60760-797 — Prednisone, 60760-840 — PREDNISONE, 61919-365 — PREDNISONE, 62135-470 — Prednisone, 62135-471 — Prednisone, 62135-553 — Prednisone, 63187-020 — Prednisone, 63187-037 — Prednisone, 63187-066 — 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.