United States · FDA National Drug Code directory
SOLU-MEDROL
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
- 0009-0039_c157d266-8633-4c2e-ae1f-0207e4f19b35
- Product NDC
- 0009-0039
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- methylprednisolone sodium succinate
- Labeler
- Pharmacia & Upjohn Company LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 19590402
- Source listing expiry
- 20261231
Source-listed ingredients
- METHYLPREDNISOLONE SODIUM SUCCINATE — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (0009-0039-28) / 1 mL in 1 VIAL (0009-0039-30) · 0009-0039-28
- 25 VIAL in 1 CARTON (0009-0039-32) / 1 mL in 1 VIAL (0009-0039-33) · 0009-0039-32
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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