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
- 17856-8815_401f96d7-592c-5df2-e063-6294a90a104d
- Product NDC
- 17856-8815
- Form
- SOLUTION
- Composition / generic term
- Prednisolone Sodium Phosphate
- Labeler
- Atlantic Biologicals Corp
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231009
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE SODIUM PHOSPHATE — 15 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSE · 17856-8815-1
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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