Prednisone

NDC 63187-807 · 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

63187-807-05 5 TABLET in 1 BOTTLE (63187-807-05)

63187-807-06 6 TABLET in 1 BOTTLE (63187-807-06)

63187-807-07 7 TABLET in 1 BOTTLE (63187-807-07)

63187-807-08 8 TABLET in 1 BOTTLE (63187-807-08)

63187-807-09 9 TABLET in 1 BOTTLE (63187-807-09)

63187-807-10 10 TABLET in 1 BOTTLE (63187-807-10)

63187-807-12 12 TABLET in 1 BOTTLE (63187-807-12)

63187-807-14 14 TABLET in 1 BOTTLE (63187-807-14)

63187-807-15 15 TABLET in 1 BOTTLE (63187-807-15)

63187-807-18 18 TABLET in 1 BOTTLE (63187-807-18)

63187-807-20 20 TABLET in 1 BOTTLE (63187-807-20)

63187-807-21 21 TABLET in 1 BOTTLE (63187-807-21)

63187-807-24 24 TABLET in 1 BOTTLE (63187-807-24)

63187-807-30 30 TABLET in 1 BOTTLE (63187-807-30)

63187-807-40 40 TABLET in 1 BOTTLE (63187-807-40)

63187-807-42 42 TABLET in 1 BOTTLE (63187-807-42)

FDA lists these products with the same active ingredient.

60760-840 — PREDNISONE, 61919-365 — PREDNISONE, 62135-470 — Prednisone, 62135-471 — Prednisone, 62135-553 — Prednisone, 63187-020 — Prednisone, 63187-037 — Prednisone, 63187-066 — Prednisone, 63187-243 — PredniSONE, 63187-300 — Prednisone, 63187-997 — Prednisone, 63561-0120 — PredniSONE, 63561-0121 — PredniSONE, 63561-0122 — PredniSONE, 63629-1605 — Prednisone, 63629-2254 — Prednisone, 63629-2257 — Prednisone, 63629-2260 — Prednisone, 63629-2264 — Prednisone, 64380-782 — PREDNISONE, +288 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.