PredniSONE
- Product NDC
- 63629-8119
- 11-digit product format
- 636298119
- Labeler code
- 63629
- Product ID
- 63629-8119_a7ac69e1-9b9c-4556-b0dc-9ae876b51c93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA080352
- Marketing category
- ANDA
- Marketing start
- 1972-04-21
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- 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 |
|---|
| 63629-8119-1 | 63629811901 | 5 TABLET in 1 BOTTLE (63629-8119-1) | 5 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8119-2 | 63629811902 | 10 TABLET in 1 BOTTLE (63629-8119-2) | 10 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8119-3 | 63629811903 | 21 TABLET in 1 BOTTLE (63629-8119-3) | 21 tablet | 2019-07-25 | 0000-00-00 | No | No | Current |