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
- 72189-589_410c34bc-cd00-f063-e063-6394a90aa7f6
- Product NDC
- 72189-589
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Direct_Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241015
- 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 (72189-589-10) · 72189-589-10
- 15 TABLET in 1 BOTTLE (72189-589-15) · 72189-589-15
- 21 TABLET in 1 BOTTLE (72189-589-21) · 72189-589-21
- 30 TABLET in 1 BOTTLE (72189-589-30) · 72189-589-30
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 →