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
- 72789-473_59965021-579f-f4e0-e063-6294a90a1b24
- Product NDC
- 72789-473
- Form
- TABLET
- Composition / generic term
- PredniSONE
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250522
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (72789-473-01) · 72789-473-01
- 4 TABLET in 1 BOTTLE, PLASTIC (72789-473-04) · 72789-473-04
- 5 TABLET in 1 BOTTLE, PLASTIC (72789-473-05) · 72789-473-05
- 10 TABLET in 1 BOTTLE, PLASTIC (72789-473-10) · 72789-473-10
- 14 TABLET in 1 BOTTLE, PLASTIC (72789-473-14) · 72789-473-14
- 15 TABLET in 1 BOTTLE, PLASTIC (72789-473-15) · 72789-473-15
- 18 TABLET in 1 BOTTLE, PLASTIC (72789-473-18) · 72789-473-18
- 20 TABLET in 1 BOTTLE, PLASTIC (72789-473-20) · 72789-473-20
- 21 TABLET in 1 BOTTLE, PLASTIC (72789-473-21) · 72789-473-21
- 25 TABLET in 1 BOTTLE, PLASTIC (72789-473-25) · 72789-473-25
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-473-30) · 72789-473-30
- 1000 TABLET in 1 BOTTLE, PLASTIC (72789-473-95) · 72789-473-95
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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