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
- 51662-1695_575f4901-bec6-37d8-e063-6394a90a060b
- Product NDC
- 51662-1695
- Form
- INJECTION
- Composition / generic term
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220324
- Source listing expiry
- 20271231
Source-listed ingredients
- METHYLPREDNISOLONE SODIUM SUCCINATE — 125 mg/2mL
These values do not establish equivalence or a dose recommendation.
Packages
Package details are not available in this snapshot.
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →