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PredniSONE Tablets, USP, 5 mg

NDC 72789-474 · PD-Rx 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

72789-474-01 — 100 TABLET in 1 BOTTLE, PLASTIC (72789-474-01)

72789-474-04 — 4 TABLET in 1 BOTTLE, PLASTIC (72789-474-04)

72789-474-21 — 21 TABLET in 1 BOTTLE, PLASTIC (72789-474-21)

72789-474-95 — 1000 TABLET in 1 BOTTLE, PLASTIC (72789-474-95)

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.

72189-589 — Prednisone, 72189-593 — Prednisone, 72189-646 — Prednisone D/P, 72189-673 — Prednisone D/P, 72789-393 — Prednisone, 72789-401 — Prednisone, 72789-413 — Prednisone, 72789-426 — PREDNISONE, 72789-448 — Prednisone, 72789-473 — PredniSONE, 72789-475 — PredniSONE, 72789-498 — PredniSONE, 72789-500 — PredniSONE, 72789-509 — PredniSONE, 72789-513 — PredniSONE, 74157-010 — Prednisone, 74157-019 — Prednisone, 76420-067 — Prednisone, 76420-068 — Prednisone, 76420-069 — 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.