United States · FDA National Drug Code directory
prednisolone sodium phosphate ODT
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
- 50742-383_ebbc1751-9381-4db1-89ff-ae5a2963fb2c
- Product NDC
- 50742-383
- Form
- TABLET, ORALLY DISINTEGRATING
- Composition / generic term
- prednisolone sodium phosphate
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20250915
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE SODIUM PHOSPHATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (50742-383-12) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (50742-383-06) · 50742-383-12
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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