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PredniSONE Tablets, USP, 20 mg

NDC 71335-2737 · Bryant Ranch Prepack

Generic namePredniSONE
Dosage formTABLET
RouteORAL
Active ingredient(s)PREDNISONE
Strength20 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

71335-2737-0 100 TABLET in 1 BOTTLE (71335-2737-0)

71335-2737-1 6 TABLET in 1 BOTTLE (71335-2737-1)

71335-2737-2 14 TABLET in 1 BOTTLE (71335-2737-2)

71335-2737-3 5 TABLET in 1 BOTTLE (71335-2737-3)

71335-2737-4 10 TABLET in 1 BOTTLE (71335-2737-4)

71335-2737-5 8 TABLET in 1 BOTTLE (71335-2737-5)

71335-2737-6 7 TABLET in 1 BOTTLE (71335-2737-6)

71335-2737-7 24 TABLET in 1 BOTTLE (71335-2737-7)

71335-2737-8 90 TABLET in 1 BOTTLE (71335-2737-8)

71335-2737-9 12 TABLET in 1 BOTTLE (71335-2737-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2079 — PREDNISONE, 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, 71335-2752 — 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, +288 more

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