NDC 0054-3722 – PredniSONE
Prednisone 5 mg/5mL · Solution · Oral
Product NDC0054-3722
Product details
- Brand name
- PredniSONE
- Generic name
- PredniSONE
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA088703
- Marketed since
- November 8, 1984
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisone 5 mg/5mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0054-3722-50 | 120 mL in 1 BOTTLE (0054-3722-50) | Dec 13, 1996 |
| 0054-3722-63 | 500 mL in 1 BOTTLE (0054-3722-63) | Nov 8, 1984 |
Recalls mentioning this NDC
- D-0008-2017 Oct 12, 2016 · Class II
Failed Tablet/Capsule Specifications: Discovery of an underweight tablet. - D-882-2013 Aug 21, 2013 · Class III
Labeling: Missing Label; missing label on blister card
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