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
- 50090-2789_a7accb10-3e0f-4102-8a4d-a3e0124e981a
- Product NDC
- 50090-2789
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19900101
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (50090-2789-1) · 50090-2789-1
- 21 TABLET in 1 BOTTLE (50090-2789-2) · 50090-2789-2
- 30 TABLET in 1 BOTTLE (50090-2789-3) · 50090-2789-3
- 100 TABLET in 1 BOTTLE (50090-2789-5) · 50090-2789-5
- 18 TABLET in 1 BOTTLE, PLASTIC (50090-2789-9) · 50090-2789-9
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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