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
- 68788-8663_36adaaf7-b451-4c6e-b36e-16ba9909c02b
- Product NDC
- 68788-8663
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240513
- 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, PLASTIC (68788-8663-1) · 68788-8663-1
- 20 TABLET in 1 BOTTLE, PLASTIC (68788-8663-2) · 68788-8663-2
- 30 TABLET in 1 BOTTLE, PLASTIC (68788-8663-3) · 68788-8663-3
- 18 TABLET in 1 BOTTLE, PLASTIC (68788-8663-4) · 68788-8663-4
- 15 TABLET in 1 BOTTLE, PLASTIC (68788-8663-5) · 68788-8663-5
- 21 TABLET in 1 BOTTLE, PLASTIC (68788-8663-8) · 68788-8663-8
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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