Prednisone
- Product NDC
- 63629-7753
- 11-digit product format
- 636297753
- Labeler code
- 63629
- Product ID
- 63629-7753_bd6475fb-0a6a-44af-a99c-6c40766adf5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA080356
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-7753-1 | 63629775301 | 12 TABLET in 1 BOTTLE (63629-7753-1) | 12 tablet | 2007-03-07 | 0000-00-00 | No | No | Current |