United States · FDA National Drug Code directory

Methylprednisolone Sodium Succinate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 63323-265_dc369096-3042-4942-9aeb-bbdf98f35bb8
Product NDC: 63323-265
Form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term: METHYLPREDNISOLONE SODIUM SUCCINATE
Labeler: Fresenius Kabi USA, LLC
Marketing category: ANDA
Marketing start / end (source format): 20041130
Source listing expiry: 20261231

Source-listed ingredients

METHYLPREDNISOLONE SODIUM SUCCINATE — 1 g/16mL

These values do not establish equivalence or a dose recommendation.

Packages

1 VIAL, MULTI-DOSE in 1 CARTON (63323-265-30) / 16 mL in 1 VIAL, MULTI-DOSE · 63323-265-30

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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