Prednisone
- Product NDC
- 63629-2259
- 11-digit product format
- 636292259
- Labeler code
- 63629
- Product ID
- 63629-2259_6ee2c359-70de-4eae-b2a3-240874de851e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2002-07-12
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 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 |
|---|
| 63629-2259-1 | 63629225901 | 500 TABLET in 1 BOTTLE, PLASTIC (63629-2259-1) | 500 tablet | 2021-03-24 | 0000-00-00 | No | No | Current |