PREDNISONE
- Product NDC
- 67296-2182
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA215672
- Marketing category
- ANDA
- Substance
- PREDNISONE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 67296-2182-1 | 10 TABLET in 1 BOTTLE (67296-2182-1) | 2022-03-28 | No | Historical | |
| 67296-2182-2 | 20 TABLET in 1 BOTTLE (67296-2182-2) | 2022-03-28 | No | Historical | |
| 67296-2182-5 | 15 TABLET in 1 BOTTLE (67296-2182-5) | 2022-03-28 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Prednisone Tablets, USP Rx only | Redpharm Drug | 2025-12-13 | HUMAN PRESCRIPTION DRUG LABEL | 2 |