prednisone

NDC 60219-1707 · Amneal Pharmaceuticals NY LLC

Generic nameprednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength10 mg/1

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

Marketing categoryANDA

Packages

60219-1707-1 — 100 TABLET in 1 BOTTLE, PLASTIC (60219-1707-1)

60219-1707-3 — 10 BLISTER PACK in 1 CARTON (60219-1707-3) / 10 TABLET in 1 BLISTER PACK (60219-1707-2)

60219-1707-5 — 500 TABLET in 1 BOTTLE, PLASTIC (60219-1707-5)

FDA lists these products with the same active ingredient.

55154-3564 — Prednisone, 55289-330 — PredniSONE, 59651-484 — PREDNISONE, 59651-485 — PREDNISONE, 59651-486 — PREDNISONE, 59651-487 — PREDNISONE, 59651-488 — PREDNISONE, 59651-489 — PREDNISONE, 60219-1705 — prednisone, 60219-1706 — 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, 60760-790 — PREDNISONE, 60760-796 — 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.