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
- 71335-2149_e6067ba3-2ab5-4c57-9fb3-1b2225069edc
- Product NDC
- 71335-2149
- 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 — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (71335-2149-0) · 71335-2149-0
- 6 TABLET in 1 BOTTLE (71335-2149-1) · 71335-2149-1
- 14 TABLET in 1 BOTTLE (71335-2149-2) · 71335-2149-2
- 5 TABLET in 1 BOTTLE (71335-2149-3) · 71335-2149-3
- 10 TABLET in 1 BOTTLE (71335-2149-4) · 71335-2149-4
- 8 TABLET in 1 BOTTLE (71335-2149-5) · 71335-2149-5
- 7 TABLET in 1 BOTTLE (71335-2149-6) · 71335-2149-6
- 24 TABLET in 1 BOTTLE (71335-2149-7) · 71335-2149-7
- 90 TABLET in 1 BOTTLE (71335-2149-8) · 71335-2149-8
- 12 TABLET in 1 BOTTLE (71335-2149-9) · 71335-2149-9
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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