Prednisolone

NDC 70404-077 · Tulex Pharmaceuticals Inc

Generic namePrednisolone oral

Dosage formSOLUTION

RouteORAL

Active ingredient(s)PREDNISOLONE

Strength15 mg/5mL

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

Marketing categoryANDA

Packages

70404-077-14 — 240 mL in 1 BOTTLE (70404-077-14)

70404-077-16 — 480 mL in 1 BOTTLE (70404-077-16)

FDA lists these products with the same active ingredient.

0121-0885 — Prednisolone, 0527-5406 — Prednisolone, 23155-927 — prednisolone oral solution, 42658-160 — PREDNISOLONE, 50090-7115 — Prednisolone, 59651-491 — PREDNISOLONE, 60722-5011 — PREDNISOLONE, 62135-250 — Prednisolone oral, 62135-437 — Prednisolone, 68999-250 — Prednisolone oral

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