PredniSONE
- Product NDC
- 50090-0102
- 11-digit product format
- 500900102
- Labeler code
- 50090
- Product ID
- 50090-0102_bd403064-43da-4220-bc99-9192730a5586
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 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 |
|---|
| 50090-0102-0 | PredniSONE | 8 in 1 BOTTLE | TABLET | 8 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0102 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 14 | Legacy NDC, 1 package rows | 20210416_ac021430-1838-4bdb-b979-795d0a09e834.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 |
|---|
| 50090-0102-0 | 50090010200 | 8 TABLET in 1 BOTTLE (50090-0102-0) | 8 tablet | 2016-06-21 | 0000-00-00 | No | No | Current |