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Prednisone

NDC 68071-3617 · 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

68071-3617-1 — 10 TABLET in 1 BOTTLE (68071-3617-1)

68071-3617-4 — 14 TABLET in 1 BOTTLE (68071-3617-4)

68071-3617-6 — 60 TABLET in 1 BOTTLE (68071-3617-6)

68071-3617-7 — 21 TABLET in 1 BOTTLE (68071-3617-7)

68071-3617-8 — 8 TABLET in 1 BOTTLE (68071-3617-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1579 — PREDNISONE, 67046-1610 — PREDNISONE, 67046-1642 — PREDNISONE, 67296-0140 — Prednisone, 67296-2081 — prednisone, 67296-2182 — PREDNISONE, 67544-399 — Prednisone, 68071-2661 — PREDNISONE, 68071-3143 — Prednisone, 68071-3581 — PredniSONE, 68071-3637 — Prednisone, 68071-3641 — PREDNISONE, 68071-3721 — PREDNISONE, 68071-3729 — PREDNISONE, 68071-3738 — PREDNISONE, 68071-3742 — PREDNISONE, 68071-3746 — PREDNISONE, 68071-3821 — Prednisone, 68071-3958 — PREDNISONE, 68071-4685 — 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.