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
- 72789-401_57c3c7f3-6773-e42a-e063-6294a90a3263
- Product NDC
- 72789-401
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191115
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE, PLASTIC (72789-401-10) · 72789-401-10
- 12 TABLET in 1 BOTTLE, PLASTIC (72789-401-12) · 72789-401-12
- 20 TABLET in 1 BOTTLE, PLASTIC (72789-401-20) · 72789-401-20
- 21 TABLET in 1 BOTTLE, PLASTIC (72789-401-21) · 72789-401-21
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-401-30) · 72789-401-30
- 40 TABLET in 1 BOTTLE, PLASTIC (72789-401-40) · 72789-401-40
- 42 TABLET in 1 BOTTLE, PLASTIC (72789-401-42) · 72789-401-42
- 50 TABLET in 1 BOTTLE, PLASTIC (72789-401-50) · 72789-401-50
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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