prednisone
- Product NDC
- 71335-2088
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209727
- Marketing category
- ANDA
- Substance
- PREDNISONE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 71335-2088-2 | 90 TABLET in 1 BOTTLE (71335-2088-2) | 20220506 | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|---|
| 07d5e455-ac3b-4890-9619-609dd0be9106 | PredniSONE Tablets USP Rx only | Bryant Ranch Prepack | 2025-03-31 | HUMAN PRESCRIPTION DRUG LABEL | 103 |