PREDNISONE

NDC 68071-3738 · NuCare Pharmaceuticals,Inc.

Generic namePREDNISONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

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

Marketing categoryANDA

Packages

68071-3738-1 — 10 TABLET in 1 BOTTLE (68071-3738-1)

68071-3738-3 — 3 TABLET in 1 BOTTLE (68071-3738-3)

68071-3738-4 — 4 TABLET in 1 BOTTLE (68071-3738-4)

68071-3738-6 — 6 TABLET in 1 BOTTLE (68071-3738-6)

FDA lists these products with the same active ingredient.

67296-2182 — PREDNISONE, 67544-399 — Prednisone, 68071-2661 — PREDNISONE, 68071-3143 — Prednisone, 68071-3581 — PredniSONE, 68071-3617 — Prednisone, 68071-3637 — Prednisone, 68071-3641 — PREDNISONE, 68071-3721 — PREDNISONE, 68071-3729 — PREDNISONE, 68071-3742 — PREDNISONE, 68071-3746 — PREDNISONE, 68071-3821 — Prednisone, 68071-3958 — PREDNISONE, 68071-4685 — Prednisone, 68788-8166 — PREDNISONE, 68788-8184 — PREDNISONE, 68788-8579 — PREDNISONE, 68788-8663 — PREDNISONE, 68788-8819 — 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.