NDC 63561-0122 – PredniSONE Tablets, USP, 20 mg
Prednisone 20 mg/1 · Tablet · Oral
Product NDC63561-0122
Product details
- Brand name
- PredniSONE Tablets, USP, 20 mg
- Generic name
- PredniSONE
- Labeler
- Granulation Technology, Inc.
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 63561-0122-1 | 100 TABLET in 1 BOTTLE (63561-0122-1) | May 22, 2025 |
| 63561-0122-2 | 1000 TABLET in 1 BOTTLE (63561-0122-2) | May 22, 2025 |
| 63561-0122-5 | 500 TABLET in 1 BOTTLE (63561-0122-5) | May 22, 2025 |
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