prednisone

NDC 64380-949 · Strides Pharma Science Limited

Generic namePREDNISONE

Dosage formTABLET

RouteORAL

Active ingredient(s)PREDNISONE

Strength50 mg/1

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

Marketing categoryANDA

Packages

64380-949-01 — 10 BLISTER PACK in 1 CARTON (64380-949-01) / 10 TABLET in 1 BLISTER PACK

64380-949-06 — 100 TABLET in 1 BOTTLE (64380-949-06)

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.

63629-1605 — Prednisone, 63629-2254 — Prednisone, 63629-2257 — Prednisone, 63629-2260 — Prednisone, 63629-2264 — Prednisone, 64380-782 — PREDNISONE, 64380-783 — PREDNISONE, 64380-784 — PREDNISONE, 64380-785 — PREDNISONE, 64380-835 — PREDNISONE, 66267-171 — Prednisone, 66267-172 — Prednisone, 66267-812 — Prednisone, 66267-860 — Prednisone, 67046-1171 — PREDNISONE, 67046-1379 — PREDNISONE, 67046-1448 — Prednisone, 67046-1579 — PREDNISONE, 67046-1610 — PREDNISONE, 67046-1642 — 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.