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
- 71205-797_0fb00b77-3fc1-4081-9540-e6a8f8e39008
- Product NDC
- 71205-797
- Form
- TABLET
- Composition / generic term
- prednisone
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200624
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE, PLASTIC (71205-797-10) · 71205-797-10
- 14 TABLET in 1 BOTTLE, PLASTIC (71205-797-14) · 71205-797-14
- 15 TABLET in 1 BOTTLE, PLASTIC (71205-797-15) · 71205-797-15
- 20 TABLET in 1 BOTTLE, PLASTIC (71205-797-20) · 71205-797-20
- 21 TABLET in 1 BOTTLE, PLASTIC (71205-797-21) · 71205-797-21
- 30 TABLET in 1 BOTTLE, PLASTIC (71205-797-30) · 71205-797-30
- 60 TABLET in 1 BOTTLE, PLASTIC (71205-797-60) · 71205-797-60
- 90 TABLET in 1 BOTTLE, PLASTIC (71205-797-90) · 71205-797-90
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 →