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
- 71335-1780_97d61269-8b46-4522-a00b-90b6eaaa19e4
- Product NDC
- 71335-1780
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191115
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 42 TABLET in 1 BOTTLE (71335-1780-0) · 71335-1780-0
- 30 TABLET in 1 BOTTLE (71335-1780-1) · 71335-1780-1
- 78 TABLET in 1 BOTTLE (71335-1780-2) · 71335-1780-2
- 36 TABLET in 1 BOTTLE (71335-1780-3) · 71335-1780-3
- 21 TABLET in 1 BOTTLE (71335-1780-4) · 71335-1780-4
- 15 TABLET in 1 BOTTLE (71335-1780-5) · 71335-1780-5
- 100 TABLET in 1 BOTTLE (71335-1780-6) · 71335-1780-6
- 20 TABLET in 1 BOTTLE (71335-1780-7) · 71335-1780-7
- 10 TABLET in 1 BOTTLE (71335-1780-8) · 71335-1780-8
- 90 TABLET in 1 BOTTLE (71335-1780-9) · 71335-1780-9
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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