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PredniSONE Tablets, USP, 5 mg

NDC 71335-2753 · Bryant Ranch Prepack

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

Packages

71335-2753-0 42 TABLET in 1 BOTTLE (71335-2753-0)

71335-2753-1 30 TABLET in 1 BOTTLE (71335-2753-1)

71335-2753-2 78 TABLET in 1 BOTTLE (71335-2753-2)

71335-2753-3 36 TABLET in 1 BOTTLE (71335-2753-3)

71335-2753-4 21 TABLET in 1 BOTTLE (71335-2753-4)

71335-2753-5 15 TABLET in 1 BOTTLE (71335-2753-5)

71335-2753-6 100 TABLET in 1 BOTTLE (71335-2753-6)

71335-2753-7 20 TABLET in 1 BOTTLE (71335-2753-7)

71335-2753-8 10 TABLET in 1 BOTTLE (71335-2753-8)

71335-2753-9 90 TABLET in 1 BOTTLE (71335-2753-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2122 — PREDNISONE, 71335-2134 — PREDNISONE, 71335-2149 — PREDNISONE, 71335-2160 — Prednisone, 71335-2273 — PREDNISONE, 71335-2356 — PREDNISONE, 71335-2389 — PREDNISONE, 71335-2736 — PredniSONE, 71335-2737 — PredniSONE, 71335-2752 — PredniSONE, 71335-2754 — PredniSONE, 71335-2895 — PREDNISONE, 71335-2938 — PredniSONE, 71335-3042 — PredniSONE, 71335-3043 — PredniSONE, 71335-3044 — PredniSONE, 71335-3045 — PredniSONE, 71335-3046 — PredniSONE, 71335-3047 — PredniSONE, 71335-3129 — 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.