prednisone

NDC 50090-7218 · A-S Medication Solutions

Generic namePREDNISONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength10 mg/1

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

Marketing categoryANDA

Packages

50090-7218-0 10 TABLET in 1 BOTTLE (50090-7218-0)

50090-7218-1 15 TABLET in 1 BOTTLE (50090-7218-1)

50090-7218-2 21 TABLET in 1 BOTTLE (50090-7218-2)

50090-7218-4 50 TABLET in 1 BOTTLE (50090-7218-4)

50090-7218-5 30 TABLET in 1 BOTTLE (50090-7218-5)

50090-7218-7 100 TABLET in 1 BOTTLE (50090-7218-7)

50090-7218-8 40 TABLET in 1 BOTTLE (50090-7218-8)

J7512 — Prednisone, immediate release or delayed release, oral, 1 mg Medicare Part B payment limit (ASP + 6%): $0.00

FDA lists these products with the same active ingredient.

50090-6225 — Prednisone, 50090-6259 — prednisone, 50090-6376 — PREDNISONE, 50090-6619 — PredniSONE, 50090-6621 — PredniSONE, 50090-6623 — PredniSONE, 50090-7023 — Prednisone, 50090-7024 — Prednisone, 50090-7025 — Prednisone, 50090-7124 — Prednisone, 50090-7219 — PREDNISONE, 50090-7235 — PREDNISONE, 50090-7369 — prednisone, 50090-7371 — prednisone, 50090-7441 — PREDNISONE, 50090-7505 — PREDNISONE, 50090-7684 — prednisone, 50090-7686 — prednisone, 50090-7688 — prednisone, 50090-7825 — 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.