NDC 0054-0019 – PredniSONE
Prednisone 50 mg/1 · Tablet · Oral
Product NDC0054-0019
Product details
- Brand name
- PredniSONE
- Generic name
- PredniSONE
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA080352
- Marketed since
- March 14, 2003
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisone 50 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0054-0019-20 | 10 BLISTER PACK in 1 CARTON (0054-0019-20) / 10 TABLET in 1 BLISTER PACK | Mar 14, 2003 |
| 0054-0019-25 | 100 TABLET in 1 BOTTLE, PLASTIC (0054-0019-25) | Mar 14, 2003 |
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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