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
- 85766-002_49ee743e-9fb2-fcb7-e063-6294a90aeefd
- Product NDC
- 85766-002
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Sportpharm LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE, PLASTIC (85766-002-00) · 85766-002-00
- 100 TABLET in 1 BOTTLE, PLASTIC (85766-002-01) · 85766-002-01
- 500 TABLET in 1 BOTTLE, PLASTIC (85766-002-05) · 85766-002-05
- 18 TABLET in 1 BOTTLE, PLASTIC (85766-002-18) · 85766-002-18
- 20 TABLET in 1 BOTTLE, PLASTIC (85766-002-20) · 85766-002-20
- 30 TABLET in 1 BOTTLE, PLASTIC (85766-002-30) · 85766-002-30
- 60 TABLET in 1 BOTTLE, PLASTIC (85766-002-60) · 85766-002-60
- 90 TABLET in 1 BOTTLE, PLASTIC (85766-002-90) · 85766-002-90
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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