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
- 70121-1001_3eb27de6-9e1c-4ef4-bb31-2458b9360582
- Product NDC
- 70121-1001
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Methylprednisolone
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161111
- 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 in 1 CARTON (70121-1001-5) / 2 mL in 1 VIAL (70121-1001-1) · 70121-1001-5
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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