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PREDNISONE

NDC 68071-3746 · NuCare Pharmaceuticals, Inc.

Generic namePREDNISONE
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength10 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

68071-3746-0 — 10 TABLET in 1 BOTTLE (68071-3746-0)

68071-3746-1 — 21 TABLET in 1 BOTTLE (68071-3746-1)

68071-3746-2 — 20 TABLET in 1 BOTTLE (68071-3746-2)

68071-3746-3 — 30 TABLET in 1 BOTTLE (68071-3746-3)

68071-3746-5 — 15 TABLET in 1 BOTTLE (68071-3746-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-2661 — PREDNISONE, 68071-3143 — Prednisone, 68071-3581 — PredniSONE, 68071-3617 — Prednisone, 68071-3637 — Prednisone, 68071-3641 — PREDNISONE, 68071-3721 — PREDNISONE, 68071-3729 — PREDNISONE, 68071-3738 — PREDNISONE, 68071-3742 — 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, 68788-8858 — PREDNISONE, 68788-8898 — PREDNISONE, +288 more

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