United States · FDA National Drug Code directory
PredniSONE Tablets, USP, 20 mg
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
- 72162-2486_34683b0d-a48c-74f4-e063-6294a90a40b4
- Product NDC
- 72162-2486
- Form
- TABLET
- Composition / generic term
- PredniSONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240306
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (72162-2486-0) · 72162-2486-0
- 100 TABLET in 1 BOTTLE (72162-2486-1) · 72162-2486-1
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 →