prednisone
- Product NDC
- 71335-2122
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208412
- Marketing category
- ANDA
- Substance
- PREDNISONE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 71335-2122-7 | 100 TABLET in 1 BOTTLE (71335-2122-7) | 20240403 | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|---|
| ecc48869-3812-4440-a398-749b28062059 | PredniSONE Tablets USP Rx only | Bryant Ranch Prepack | 2025-09-29 | HUMAN PRESCRIPTION DRUG LABEL | 104 |