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METHYLPREDNISOLONE

NDC 70518-2864 · REMEDYREPACK INC.

Generic nameMETHYLPREDNISOLONE
Dosage formTABLET
RouteORAL
Active ingredient(s)METHYLPREDNISOLONE
Strength4 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

70518-2864-0 — 1 BLISTER PACK in 1 CARTON (70518-2864-0) / 21 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-624 — methylprednisolone, 68071-2370 — methylprednisolone, 68071-5221 — METHYLPREDNISOLONE, 68084-149 — Methylprednisolone, 68382-916 — methylprednisolone, 68382-917 — methylprednisolone, 68382-918 — methylprednisolone, 68382-919 — methylprednisolone, 68788-7833 — METHYLPREDNISOLONE, 69306-400 — METHYLPREDNISOLONE, 70518-4213 — methylprednisolone, 70771-1348 — methylprednisolone, 70771-1349 — methylprednisolone, 70771-1350 — methylprednisolone, 70771-1351 — methylprednisolone, 71205-453 — METHYLPREDNISOLONE, 72162-1161 — methylprednisolone, 72189-264 — METHYLPREDNISOLONE, 76420-041 — Methylprednisolone, 76420-193 — METHYLPREDNISOLONE, +31 more

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