Skip to main content

PredniSONE Tablets, USP, 10 mg

NDC 71335-2752 · Bryant Ranch Prepack

Generic namePredniSONE
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength10 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

71335-2752-0 10 TABLET in 1 BOTTLE (71335-2752-0)

71335-2752-1 21 TABLET in 1 BOTTLE (71335-2752-1)

71335-2752-2 40 TABLET in 1 BOTTLE (71335-2752-2)

71335-2752-3 30 TABLET in 1 BOTTLE (71335-2752-3)

71335-2752-4 20 TABLET in 1 BOTTLE (71335-2752-4)

71335-2752-5 15 TABLET in 1 BOTTLE (71335-2752-5)

71335-2752-6 50 TABLET in 1 BOTTLE (71335-2752-6)

71335-2752-7 60 TABLET in 1 BOTTLE (71335-2752-7)

71335-2752-8 42 TABLET in 1 BOTTLE (71335-2752-8)

71335-2752-9 48 TABLET in 1 BOTTLE (71335-2752-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2088 — PREDNISONE, 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, 71335-2753 — 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, +288 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.