NDC 71335-2737 – PredniSONE Tablets, USP, 20 mg
Prednisone 20 mg/1 · Tablet · Oral
Product NDC71335-2737
Product details
- Brand name
- PredniSONE Tablets, USP, 20 mg
- Generic name
- PredniSONE
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA212629
- Marketed since
- May 22, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisone 20 mg/1
Uses, dosage, side effects and warnings for PredniSONE Tablets, USP, 20 mg →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2737-0 | 100 TABLET in 1 BOTTLE (71335-2737-0) | Sep 26, 2025 |
| 71335-2737-1 | 6 TABLET in 1 BOTTLE (71335-2737-1) | Sep 26, 2025 |
| 71335-2737-2 | 14 TABLET in 1 BOTTLE (71335-2737-2) | Sep 26, 2025 |
| 71335-2737-3 | 5 TABLET in 1 BOTTLE (71335-2737-3) | Sep 26, 2025 |
| 71335-2737-4 | 10 TABLET in 1 BOTTLE (71335-2737-4) | Sep 26, 2025 |
| 71335-2737-5 | 8 TABLET in 1 BOTTLE (71335-2737-5) | Sep 26, 2025 |
| 71335-2737-6 | 7 TABLET in 1 BOTTLE (71335-2737-6) | Sep 26, 2025 |
| 71335-2737-7 | 24 TABLET in 1 BOTTLE (71335-2737-7) | Sep 26, 2025 |
| 71335-2737-8 | 90 TABLET in 1 BOTTLE (71335-2737-8) | Sep 26, 2025 |
| 71335-2737-9 | 12 TABLET in 1 BOTTLE (71335-2737-9) | Sep 26, 2025 |
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