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
- 50090-6123_77958ed5-1eaa-43ab-afcf-a380652a664f
- Product NDC
- 50090-6123
- Form
- TABLET
- Composition / generic term
- prednisone
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200624
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE (50090-6123-0) · 50090-6123-0
- 12 TABLET in 1 BOTTLE (50090-6123-1) · 50090-6123-1
- 6 TABLET in 1 BOTTLE (50090-6123-2) · 50090-6123-2
- 14 TABLET in 1 BOTTLE (50090-6123-5) · 50090-6123-5
- 15 TABLET in 1 BOTTLE (50090-6123-7) · 50090-6123-7
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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