PredniSONE
- Product NDC
- 63629-4562
- 11-digit product format
- 636294562
- Labeler code
- 63629
- Product ID
- 63629-4562_7da4f0d2-a811-4c4c-9667-242cef340917
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA084283
- Marketing category
- ANDA
- Marketing start
- 2003-03-14
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4562-1 | 63629456201 | 90 TABLET in 1 BOTTLE (63629-4562-1) | 90 tablet | 2011-08-19 | 0000-00-00 | No | No | Current |
| 63629-4562-2 | 63629456202 | 5 TABLET in 1 BOTTLE (63629-4562-2) | 5 tablet | 2014-01-02 | 0000-00-00 | No | No | Current |
| 63629-4562-3 | 63629456203 | 30 TABLET in 1 BOTTLE (63629-4562-3) | 30 tablet | 2014-08-14 | 0000-00-00 | No | No | Current |
| 63629-4562-4 | 63629456204 | 60 TABLET in 1 BOTTLE (63629-4562-4) | 60 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-4562-5 | 63629456205 | 120 TABLET in 1 BOTTLE (63629-4562-5) | 120 tablet | 2021-12-22 | 0000-00-00 | No | No | Current |
| 63629-4562-6 | 63629456206 | 7 TABLET in 1 BOTTLE (63629-4562-6) | 7 tablet | 2017-05-03 | 0000-00-00 | No | No | Current |
| 63629-4562-7 | 63629456207 | 20 TABLET in 1 BOTTLE (63629-4562-7) | 20 tablet | 2018-06-25 | 0000-00-00 | No | No | Current |