Prednisone

NDC 60687-134 · American Health Packaging

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength10 mg/1

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

Marketing categoryANDA

Packages

60687-134-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-134-01) / 1 TABLET in 1 BLISTER PACK (60687-134-11)

J7512 — Prednisone, immediate release or delayed release, oral, 1 mg Medicare Part B payment limit (ASP + 6%): $0.00

FDA lists these products with the same active ingredient.

59651-485 — PREDNISONE, 59651-486 — PREDNISONE, 59651-487 — PREDNISONE, 59651-488 — PREDNISONE, 59651-489 — PREDNISONE, 60219-1705 — prednisone, 60219-1706 — prednisone, 60219-1707 — prednisone, 60219-1708 — prednisone, 60687-122 — Prednisone, 60687-145 — Prednisone, 60687-854 — Prednisone, 60687-903 — PREDNISONE, 60687-914 — Prednisone, 60687-925 — Prednisone, 60760-790 — PREDNISONE, 60760-796 — PredniSONE, 60760-797 — Prednisone, 60760-840 — PREDNISONE, 61919-365 — 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.