PredniSONE
- Product NDC
- 63629-6660
- 11-digit product format
- 636296660
- Labeler code
- 63629
- Product ID
- 63629-6660_017b9466-57f2-41e2-863b-75c67957cf57
- 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
- 2021-12-31
- 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 |
|---|
| 63629-6660-1 | 63629666001 | 5 TABLET in 1 BOTTLE (63629-6660-1) | 5 tablet | 2015-08-10 | 0000-00-00 | No | No | Current |