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prednisone

NDC 51655-988 · Northwind Health Company, LLC

Generic nameprednisone
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength5 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

51655-988-21 — 21 TABLET in 1 BOTTLE, PLASTIC (51655-988-21)

51655-988-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-988-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-410 — Prednisone, 51655-493 — PredniSONE, 51655-541 — PREDNISONE, 51655-701 — PredniSONE, 51655-726 — PredniSONE, 51655-763 — PredniSONE, 51655-765 — Prednisone, 51655-935 — Prednisone, 51655-939 — PredniSONE, 51655-972 — PREDNISONE, 54348-506 — PREDNISONE, 55154-2146 — Prednisone, 55154-2147 — Prednisone, 55154-2581 — Prednisone, 55154-2582 — PREDNISONE, 55154-3564 — Prednisone, 55289-330 — PredniSONE, 59651-484 — PREDNISONE, 59651-485 — PREDNISONE, 59651-486 — 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.