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
- 43598-129_9846244f-7189-5a82-a2aa-8f123805ee1f
- Product NDC
- 43598-129
- Form
- INJECTION
- Composition / generic term
- Methylprednisolone sodium succinate
- Labeler
- Dr. Reddy's Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220324
- Source listing expiry
- 20261231
Source-listed ingredients
- METHYLPREDNISOLONE SODIUM SUCCINATE — 125 mg/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 CARTON (43598-129-25) / 2 mL in 1 VIAL, SINGLE-DOSE (43598-129-01) · 43598-129-25
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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