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
- 70404-077_561d8c9c-b67f-7fb2-e063-6394a90a0316
- Product NDC
- 70404-077
- Form
- SOLUTION
- Composition / generic term
- Prednisolone oral
- Labeler
- Tulex Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260708
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISOLONE — 15 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 240 mL in 1 BOTTLE (70404-077-14) · 70404-077-14
- 480 mL in 1 BOTTLE (70404-077-16) · 70404-077-16
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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