PREDNISONE
- Product NDC
- 50090-7441
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215672
- Marketing category
- ANDA
- Substance
- PREDNISONE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-7441-0 | 8 TABLET in 1 BOTTLE (50090-7441-0) | 2024-11-06 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Prednisone Tablets, USP Rx only | A-S Medication Solutions | 2024-11-08 | Human Prescription Drug Label | 1 |