prednisone

NDC 68788-8663 · Preferred 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

68788-8663-1 — 10 TABLET in 1 BOTTLE, PLASTIC (68788-8663-1)

68788-8663-2 — 20 TABLET in 1 BOTTLE, PLASTIC (68788-8663-2)

68788-8663-3 — 30 TABLET in 1 BOTTLE, PLASTIC (68788-8663-3)

68788-8663-4 — 18 TABLET in 1 BOTTLE, PLASTIC (68788-8663-4)

68788-8663-5 — 15 TABLET in 1 BOTTLE, PLASTIC (68788-8663-5)

68788-8663-8 — 21 TABLET in 1 BOTTLE, PLASTIC (68788-8663-8)

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

FDA lists these products with the same active ingredient.

68071-3729 — PREDNISONE, 68071-3738 — PREDNISONE, 68071-3742 — PREDNISONE, 68071-3746 — PREDNISONE, 68071-3821 — Prednisone, 68071-3958 — PREDNISONE, 68071-4685 — Prednisone, 68788-8166 — PREDNISONE, 68788-8184 — PREDNISONE, 68788-8579 — 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, 70518-3539 — PREDNISONE, 70518-3540 — 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.