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
- 0121-0773_cdc1335b-41fb-4df2-b201-69150adbb03d
- Product NDC
- 0121-0773
- Form
- SOLUTION
- Composition / generic term
- Prednisolone Sodium Phosphate
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170131
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE SODIUM PHOSPHATE — 10 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 237 mL in 1 BOTTLE (0121-0773-08) · 0121-0773-08
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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