PREDNISONE

NDC 68071-3729 · NuCare Pharmaceuticals,Inc.

Generic namePREDNISONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength5 mg/1

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

Marketing categoryANDA

Packages

68071-3729-1 — 21 TABLET in 1 BOTTLE (68071-3729-1)

68071-3729-2 — 20 TABLET in 1 BOTTLE (68071-3729-2)

68071-3729-5 — 15 TABLET in 1 BOTTLE (68071-3729-5)

68071-3729-9 — 90 TABLET in 1 BOTTLE (68071-3729-9)

FDA lists these products with the same active ingredient.

67296-2081 — prednisone, 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, 68071-3738 — 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, +288 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.