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
- 85766-086_503196db-b234-c296-e063-6394a90ae483
- Product NDC
- 85766-086
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Sportpharm LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220524
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (85766-086-01) · 85766-086-01
- 5 TABLET in 1 BOTTLE (85766-086-05) · 85766-086-05
- 10 TABLET in 1 BOTTLE (85766-086-10) · 85766-086-10
- 20 TABLET in 1 BOTTLE (85766-086-20) · 85766-086-20
- 30 TABLET in 1 BOTTLE (85766-086-30) · 85766-086-30
- 60 TABLET in 1 BOTTLE (85766-086-60) · 85766-086-60
- 90 TABLET in 1 BOTTLE (85766-086-90) · 85766-086-90
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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