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
- 68788-8166_c1619b4a-e3d3-4690-a9ee-cb0721ab898d
- Product NDC
- 68788-8166
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220408
- 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 (68788-8166-1) · 68788-8166-1
- 21 TABLET in 1 BOTTLE (68788-8166-2) · 68788-8166-2
- 30 TABLET in 1 BOTTLE (68788-8166-3) · 68788-8166-3
- 40 TABLET in 1 BOTTLE (68788-8166-4) · 68788-8166-4
- 50 TABLET in 1 BOTTLE (68788-8166-5) · 68788-8166-5
- 15 TABLET in 1 BOTTLE (68788-8166-6) · 68788-8166-6
- 45 TABLET in 1 BOTTLE (68788-8166-7) · 68788-8166-7
- 20 TABLET in 1 BOTTLE (68788-8166-8) · 68788-8166-8
- 90 TABLET in 1 BOTTLE (68788-8166-9) · 68788-8166-9
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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