PREDNISONE
- Product NDC
- 50090-5453
- 11-digit product format
- 500905453
- Labeler code
- 50090
- Product ID
- 50090-5453_e645501c-2c95-4133-b68c-f7f1209d9927
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5453-0 | 50090545300 | 21 TABLET in 1 BOTTLE (50090-5453-0) | 21 tablet | 2021-01-26 | 0000-00-00 | No | No | Current |