United States · FDA National Drug Code directory
Solu-Cortef
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
- 0009-0016_4e9814fe-3089-4980-a207-bf0aa95d4c36
- Product NDC
- 0009-0016
- Form
- INJECTION, POWDER, FOR SOLUTION
- Composition / generic term
- hydrocortisone sodium succinate
- Labeler
- Pharmacia & Upjohn Company LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 19550427
- Source listing expiry
- 20271231
Source-listed ingredients
- HYDROCORTISONE SODIUM SUCCINATE — 500 mg/4mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (0009-0016-12) / 4 mL in 1 VIAL, SINGLE-DOSE · 0009-0016-12
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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