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SOLU-MEDROL

NDC 71872-7061 · Medical Purchasing Solutions, LLC

Generic namemethylprednisolone sodium succinate
Dosage formINJECTION, POWDER, FOR SOLUTION
RouteINTRAMUSCULAR, INTRAVENOUS
Active ingredient(s)METHYLPREDNISOLONE SODIUM SUCCINATE
Strength125 mg/2mL
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryNDA

Packages

71872-7061-1 — 1 VIAL in 1 BAG (71872-7061-1) / 2 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-3941 — methylprednisolone sodium succinate, 55154-3944 — methylprednisolone sodium succinate, 63323-255 — METHYLPREDNISOLONE SODIUM SUCCINATE, 63323-258 — METHYLPREDNISOLONE SODIUM SUCCINATE, 63323-265 — METHYLPREDNISOLONE SODIUM SUCCINATE, 70121-1000 — Methylprednisolone, 70121-1001 — Methylprednisolone, 70518-2023 — methylprednisolone sodium succinate, 70518-3684 — Methylprednisolone sodium succinate, 70518-4345 — Methylprednisolone Sodium Succinate, 71872-7085 — methylprednisolone sodium succinate, 71872-7232 — methylprednisolone sodium succinate, 72572-097 — Methylprednisolone Sodium Succinate, 72572-098 — Methylprednisolone Sodium Succinate, 82094-401 — Methylprednisolone, 82094-402 — Methylprednisolone, 82094-403 — Methylprednisolone, 82094-404 — Methylprednisolone, 82094-405 — Methylprednisolone, 84549-039 — methylprednisolone sodium succinate, +31 more

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