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
- 68999-330_453ad2a6-3423-b21b-e063-6294a90abb44
- Product NDC
- 68999-330
- Form
- SOLUTION
- Composition / generic term
- prednisolone sodium phosphate
- Labeler
- Chartwell Governmental & Specialty RX, LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040525
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE SODIUM PHOSPHATE — 5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TRAY in 1 BOX (68999-330-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-330-05) · 68999-330-24
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 →