United States · FDA National Drug Code directory
PredniSONE
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
- 0054-3722_523ad364-8d95-4679-9290-446d61f36eb5
- Product NDC
- 0054-3722
- Form
- SOLUTION
- Composition / generic term
- PredniSONE
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19841108
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 5 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 120 mL in 1 BOTTLE (0054-3722-50) · 0054-3722-50
- 500 mL in 1 BOTTLE (0054-3722-63) · 0054-3722-63
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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