Prednisone

NDC 71205-239 · Proficient Rx LP

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength20 mg/1

Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

Marketing categoryANDA

Packages

71205-239-05 5 TABLET in 1 BOTTLE (71205-239-05)

71205-239-06 6 TABLET in 1 BOTTLE (71205-239-06)

71205-239-07 7 TABLET in 1 BOTTLE (71205-239-07)

71205-239-10 10 TABLET in 1 BOTTLE (71205-239-10)

71205-239-12 12 TABLET in 1 BOTTLE (71205-239-12)

71205-239-14 14 TABLET in 1 BOTTLE (71205-239-14)

71205-239-15 15 TABLET in 1 BOTTLE (71205-239-15)

71205-239-18 18 TABLET in 1 BOTTLE (71205-239-18)

71205-239-20 20 TABLET in 1 BOTTLE (71205-239-20)

71205-239-21 21 TABLET in 1 BOTTLE (71205-239-21)

71205-239-30 30 TABLET in 1 BOTTLE (71205-239-30)

71205-239-60 60 TABLET in 1 BOTTLE (71205-239-60)

71205-239-90 90 TABLET in 1 BOTTLE (71205-239-90)

FDA lists these products with the same active ingredient.

70518-4354 — prednisone, 70518-4560 — PREDNISONE, 70518-4660 — PREDNISONE, 70954-056 — Prednisone, 70954-057 — Prednisone, 70954-058 — Prednisone, 70954-059 — Prednisone, 70954-060 — Prednisone, 70954-061 — Prednisone, 71205-089 — Prednisone, 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, +288 more

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