prednisone

NDC 67046-1579 · Coupler LLC

Generic namePREDNISONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength10 mg/1

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

Marketing categoryANDA

Packages

67046-1579-3 — 30 TABLET in 1 BLISTER PACK (67046-1579-3)

FDA lists these products with the same active ingredient.

64380-785 — PREDNISONE, 64380-835 — PREDNISONE, 64380-949 — PREDNISONE, 66267-171 — Prednisone, 66267-172 — Prednisone, 66267-812 — Prednisone, 66267-860 — Prednisone, 67046-1171 — PREDNISONE, 67046-1379 — PREDNISONE, 67046-1448 — Prednisone, 67046-1610 — PREDNISONE, 67046-1642 — PREDNISONE, 67296-0140 — Prednisone, 67296-2081 — prednisone, 67296-2182 — PREDNISONE, 67544-399 — Prednisone, 68071-2661 — PREDNISONE, 68071-3143 — Prednisone, 68071-3581 — PredniSONE, 68071-3617 — 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.