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
- 71335-2754_fd21957e-bea4-4025-9058-bcdd33d032ad
- Product NDC
- 71335-2754
- 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
- 11 TABLET in 1 BOTTLE (71335-2754-0) · 71335-2754-0
- 20 TABLET in 1 BOTTLE (71335-2754-1) · 71335-2754-1
- 30 TABLET in 1 BOTTLE (71335-2754-2) · 71335-2754-2
- 40 TABLET in 1 BOTTLE (71335-2754-3) · 71335-2754-3
- 15 TABLET in 1 BOTTLE (71335-2754-4) · 71335-2754-4
- 10 TABLET in 1 BOTTLE (71335-2754-5) · 71335-2754-5
- 21 TABLET in 1 BOTTLE (71335-2754-6) · 71335-2754-6
- 18 TABLET in 1 BOTTLE (71335-2754-7) · 71335-2754-7
- 12 TABLET in 1 BOTTLE (71335-2754-8) · 71335-2754-8
- 23 TABLET in 1 BOTTLE (71335-2754-9) · 71335-2754-9
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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