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
- 60722-5011_da9dfcf4-1631-4923-9536-72c27fc0b307
- Product NDC
- 60722-5011
- Form
- TABLET
- Composition / generic term
- PREDNISOLONE
- Labeler
- Zhejiang Xianju Pharmaceutical Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240901
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISOLONE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (60722-5011-0) · 60722-5011-0
- 1000 TABLET in 1 BOTTLE (60722-5011-1) · 60722-5011-1
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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