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prednisone

NDC 71335-2069 · 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

71335-2069-0 10 TABLET in 1 BOTTLE (71335-2069-0)

71335-2069-1 21 TABLET in 1 BOTTLE (71335-2069-1)

71335-2069-2 40 TABLET in 1 BOTTLE (71335-2069-2)

71335-2069-3 30 TABLET in 1 BOTTLE (71335-2069-3)

71335-2069-4 20 TABLET in 1 BOTTLE (71335-2069-4)

71335-2069-5 15 TABLET in 1 BOTTLE (71335-2069-5)

71335-2069-6 50 TABLET in 1 BOTTLE (71335-2069-6)

71335-2069-7 60 TABLET in 1 BOTTLE (71335-2069-7)

71335-2069-8 42 TABLET in 1 BOTTLE (71335-2069-8)

71335-2069-9 48 TABLET in 1 BOTTLE (71335-2069-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-362 — Prednisone, 71205-407 — Prednisone, 71205-421 — Prednisone, 71205-665 — Prednisone, 71205-729 — PREDNISONE, 71205-741 — PREDNISONE, 71205-755 — PREDNISONE, 71205-797 — prednisone, 71205-818 — prednisone, 71335-1780 — Prednisone, 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, +288 more

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