NDC 68788-4182 – PredniSONE
Prednisone 20 mg/1 · Tablet · Oral
Product NDC68788-4182
Product details
- Brand name
- PredniSONE
- Generic name
- PredniSONE
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA080352
- Marketed since
- August 20, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Corticosteroid
Active ingredients
- Prednisone 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68788-4182-1 | 10 TABLET in 1 BOTTLE, PLASTIC (68788-4182-1) | Aug 20, 2026 |
| 68788-4182-2 | 20 TABLET in 1 BOTTLE, PLASTIC (68788-4182-2) | Aug 20, 2026 |
| 68788-4182-3 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-4182-3) | Aug 20, 2026 |
| 68788-4182-4 | 18 TABLET in 1 BOTTLE, PLASTIC (68788-4182-4) | Aug 20, 2026 |
| 68788-4182-5 | 15 TABLET in 1 BOTTLE, PLASTIC (68788-4182-5) | Aug 20, 2026 |
| 68788-4182-8 | 21 TABLET in 1 BOTTLE, PLASTIC (68788-4182-8) | Aug 20, 2026 |
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