United States · FDA National Drug Code directory
PredniSONE Tablets, USP, 20 mg
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
- 71335-2737_312a41b9-2327-405a-b39d-40594fdc4eae
- Product NDC
- 71335-2737
- Form
- TABLET
- Composition / generic term
- PredniSONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250522
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (71335-2737-0) · 71335-2737-0
- 6 TABLET in 1 BOTTLE (71335-2737-1) · 71335-2737-1
- 14 TABLET in 1 BOTTLE (71335-2737-2) · 71335-2737-2
- 5 TABLET in 1 BOTTLE (71335-2737-3) · 71335-2737-3
- 10 TABLET in 1 BOTTLE (71335-2737-4) · 71335-2737-4
- 8 TABLET in 1 BOTTLE (71335-2737-5) · 71335-2737-5
- 7 TABLET in 1 BOTTLE (71335-2737-6) · 71335-2737-6
- 24 TABLET in 1 BOTTLE (71335-2737-7) · 71335-2737-7
- 90 TABLET in 1 BOTTLE (71335-2737-8) · 71335-2737-8
- 12 TABLET in 1 BOTTLE (71335-2737-9) · 71335-2737-9
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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