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
- 71335-2122_2fb6d261-a018-44c0-883c-45f64f06ded6
- Product NDC
- 71335-2122
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 TABLET in 1 BOTTLE (71335-2122-0) · 71335-2122-0
- 5 TABLET in 1 BOTTLE (71335-2122-1) · 71335-2122-1
- 54 TABLET in 1 BOTTLE (71335-2122-2) · 71335-2122-2
- 90 TABLET in 1 BOTTLE (71335-2122-3) · 71335-2122-3
- 18 TABLET in 1 BOTTLE (71335-2122-4) · 71335-2122-4
- 25 TABLET in 1 BOTTLE (71335-2122-5) · 71335-2122-5
- 26 TABLET in 1 BOTTLE (71335-2122-6) · 71335-2122-6
- 100 TABLET in 1 BOTTLE (71335-2122-7) · 71335-2122-7
- 24 TABLET in 1 BOTTLE (71335-2122-8) · 71335-2122-8
- 16 TABLET in 1 BOTTLE (71335-2122-9) · 71335-2122-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →