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
- 71205-665_35f504c3-1cf5-455d-8226-9ffeea606623
- Product NDC
- 71205-665
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191115
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET in 1 BOTTLE (71205-665-05) · 71205-665-05
- 10 TABLET in 1 BOTTLE (71205-665-10) · 71205-665-10
- 20 TABLET in 1 BOTTLE (71205-665-20) · 71205-665-20
- 21 TABLET in 1 BOTTLE (71205-665-21) · 71205-665-21
- 24 TABLET in 1 BOTTLE (71205-665-24) · 71205-665-24
- 30 TABLET in 1 BOTTLE (71205-665-30) · 71205-665-30
- 60 TABLET in 1 BOTTLE (71205-665-60) · 71205-665-60
- 90 TABLET in 1 BOTTLE (71205-665-90) · 71205-665-90
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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