METHYLPREDNISOLONE

NDC 57582-101 · Tianjin Tianyao Pharmaceuticals Co., Ltd.

Generic nameMETHYLPREDNISOLONE

Dosage formTABLET

RouteORAL

Active ingredient(s)METHYLPREDNISOLONE

Strength4 mg/1

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

Marketing categoryANDA

Packages

57582-101-01 — 100 TABLET in 1 BOTTLE (57582-101-01)

57582-101-02 — 1 BLISTER PACK in 1 CARTON (57582-101-02) / 21 TABLET in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

0009-0020 — methylprednisolone, 0009-0022 — methylprednisolone, 0009-0056 — methylprednisolone, 0009-0073 — methylprednisolone, 0603-4593 — methylprednisolone, 0904-6914 — methylprednisolone, 42806-400 — METHYLPREDNISOLONE, 50090-3094 — Methylprednisolone, 50090-3811 — methylprednisolone, 55289-649 — methylprednisolone, 59762-0049 — methylprednisolone, 59762-0050 — methylprednisolone, 59762-0051 — methylprednisolone, 59762-4440 — methylprednisolone, 60760-961 — METHYLPREDNISOLONE, 62135-759 — Methylprednisolone, 62135-760 — Methylprednisolone, 62135-761 — Methylprednisolone, 62135-762 — Methylprednisolone, 62135-763 — Methylprednisolone, +31 more

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