United States · FDA National Drug Code directory
Prednisolone Sodium Phosphate
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
- 13925-166_da94c24a-0943-4544-8286-467d7c073c34
- Product NDC
- 13925-166
- Form
- SOLUTION
- Composition / generic term
- Prednisolone Sodium Phosphate
- Labeler
- Seton Pharmaceuticals, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20131018
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE SODIUM PHOSPHATE — 5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 120 mL in 1 BOTTLE (13925-166-04) · 13925-166-04
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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