Prednisone
- Product NDC
- 50090-2608
- 11-digit product format
- 500902608
- Labeler code
- 50090
- Product ID
- 50090-2608_014acf9a-5ab1-4cc1-989b-390ed0e1d3e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA085162
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2608-0 | Prednisone | 60 in 1 BOTTLE | TABLET | 60 | | 36 |
| 50090-2608-1 | Prednisone | 20 in 1 BOTTLE | TABLET | 20 | | 36 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2608 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 33 | Legacy NDC, 2 package rows | 20210206_de498de3-6ee6-4594-895e-cc69f050e34e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2608-0 | 50090260800 | 60 TABLET in 1 BOTTLE (50090-2608-0) | 60 tablet | 2016-12-02 | 0000-00-00 | No | No | Current |
| 50090-2608-1 | 50090260801 | 20 TABLET in 1 BOTTLE (50090-2608-1) | 20 tablet | 2016-11-09 | 0000-00-00 | No | No | Current |