United States · FDA National Drug Code directory
PredniSONE Tablets, USP, 5 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
- 71335-2753_d41fab26-b03f-4bee-a72a-06829cf538d7
- Product NDC
- 71335-2753
- 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 — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 42 TABLET in 1 BOTTLE (71335-2753-0) · 71335-2753-0
- 30 TABLET in 1 BOTTLE (71335-2753-1) · 71335-2753-1
- 78 TABLET in 1 BOTTLE (71335-2753-2) · 71335-2753-2
- 36 TABLET in 1 BOTTLE (71335-2753-3) · 71335-2753-3
- 21 TABLET in 1 BOTTLE (71335-2753-4) · 71335-2753-4
- 15 TABLET in 1 BOTTLE (71335-2753-5) · 71335-2753-5
- 100 TABLET in 1 BOTTLE (71335-2753-6) · 71335-2753-6
- 20 TABLET in 1 BOTTLE (71335-2753-7) · 71335-2753-7
- 10 TABLET in 1 BOTTLE (71335-2753-8) · 71335-2753-8
- 90 TABLET in 1 BOTTLE (71335-2753-9) · 71335-2753-9
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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