United States · FDA National Drug Code directory
Prednisolone
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
- 50090-7115_9a49f696-0cdf-45d7-adc4-f1cb1fbb690b
- Product NDC
- 50090-7115
- Form
- SOLUTION
- Composition / generic term
- Prednisolone
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230912
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISOLONE — 15 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE, DISPENSING in 1 BOTTLE (50090-7115-0) / 120 mL in 1 BOTTLE, DISPENSING · 50090-7115-0
- 4 BOTTLE, DISPENSING in 1 BOTTLE (50090-7115-1) / 60 mL in 1 BOTTLE, DISPENSING · 50090-7115-1
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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