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
- 71335-2069_7d233ed2-f92f-48f1-bd5a-8bf14eddae42
- Product NDC
- 71335-2069
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (71335-2069-0) · 71335-2069-0
- 21 TABLET in 1 BOTTLE (71335-2069-1) · 71335-2069-1
- 40 TABLET in 1 BOTTLE (71335-2069-2) · 71335-2069-2
- 30 TABLET in 1 BOTTLE (71335-2069-3) · 71335-2069-3
- 20 TABLET in 1 BOTTLE (71335-2069-4) · 71335-2069-4
- 15 TABLET in 1 BOTTLE (71335-2069-5) · 71335-2069-5
- 50 TABLET in 1 BOTTLE (71335-2069-6) · 71335-2069-6
- 60 TABLET in 1 BOTTLE (71335-2069-7) · 71335-2069-7
- 42 TABLET in 1 BOTTLE (71335-2069-8) · 71335-2069-8
- 48 TABLET in 1 BOTTLE (71335-2069-9) · 71335-2069-9
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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