Prednisone

NDC 71205-665 · Proficient Rx LP

Generic namePrednisone

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength50 mg/1

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

Marketing categoryANDA

Packages

71205-665-05 5 TABLET in 1 BOTTLE (71205-665-05)

71205-665-10 10 TABLET in 1 BOTTLE (71205-665-10)

71205-665-20 20 TABLET in 1 BOTTLE (71205-665-20)

71205-665-21 21 TABLET in 1 BOTTLE (71205-665-21)

71205-665-24 24 TABLET in 1 BOTTLE (71205-665-24)

71205-665-30 30 TABLET in 1 BOTTLE (71205-665-30)

71205-665-60 60 TABLET in 1 BOTTLE (71205-665-60)

71205-665-90 90 TABLET in 1 BOTTLE (71205-665-90)

FDA lists these products with the same active ingredient.

70954-057 — Prednisone, 70954-058 — Prednisone, 70954-059 — Prednisone, 70954-060 — Prednisone, 70954-061 — Prednisone, 71205-089 — Prednisone, 71205-239 — Prednisone, 71205-362 — Prednisone, 71205-407 — Prednisone, 71205-421 — Prednisone, 71205-729 — PREDNISONE, 71205-741 — PREDNISONE, 71205-755 — PREDNISONE, 71205-797 — prednisone, 71205-818 — prednisone, 71335-1780 — Prednisone, 71335-2069 — PREDNISONE, 71335-2079 — PREDNISONE, 71335-2088 — PREDNISONE, 71335-2122 — 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.