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prednisone

NDC 68788-8184 · Preferred Pharmaceuticals Inc.

Generic namePREDNISONE
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength2.5 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

68788-8184-1 — 15 TABLET in 1 BOTTLE (68788-8184-1)

68788-8184-3 — 30 TABLET in 1 BOTTLE (68788-8184-3)

Billed under HCPCS

J7512 — Prednisone, immediate release or delayed release, oral, 1 mg Medicare Part B payment limit (ASP + 6%): $0.00

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68788-8166 — PREDNISONE, 68788-8579 — PREDNISONE, 68788-8663 — PREDNISONE, 68788-8819 — PREDNISONE, 68788-8858 — PREDNISONE, 68788-8898 — PREDNISONE, 68788-9551 — Prednisone, 70518-0305 — Prednisone, 70518-3401 — PREDNISONE, 70518-3476 — PREDNISONE, 70518-3537 — 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.