NDC 0054-3721 – PredniSONE Intensol
Prednisone 5 mg/mL · Solution, Concentrate · Oral
Product NDC0054-3721
Product details
- Brand name
- PredniSONE Intensol
- Generic name
- PredniSONE Intensol
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Solution, Concentrate
- Route
- Oral
- Marketing category
- ANDA · ANDA088810
- Marketed since
- February 20, 1985
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisone 5 mg/mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0054-3721-44 | 30 mL in 1 BOTTLE, GLASS (0054-3721-44) | Feb 20, 1985 |
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