Prednisone
- Product NDC
- 50090-3330
- 11-digit product format
- 500903330
- Labeler code
- 50090
- Product ID
- 50090-3330_15b13f56-0d84-444c-a4a1-2d635596db4e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2001-08-29
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3330 | PREDNISONE (PREDNISONE) TABLET [A-S MEDICATION SOLUTIONS] | 21 | Legacy NDC, 5 package rows | 20240627_751b7f62-f92b-4b7c-a588-2c882d5d1ce3.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 |
|---|
| 50090-3330-0 | 50090333000 | 20 TABLET in 1 BOTTLE (50090-3330-0) | 20 tablet | 2018-01-12 | 0000-00-00 | No | No | Current |
| 50090-3330-1 | 50090333001 | 12 TABLET in 1 BOTTLE (50090-3330-1) | 12 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |
| 50090-3330-2 | 50090333002 | 6 TABLET in 1 BOTTLE (50090-3330-2) | 6 tablet | 2022-06-29 | 0000-00-00 | No | No | Current |
| 50090-3330-5 | 50090333005 | 14 TABLET in 1 BOTTLE (50090-3330-5) | 14 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |
| 50090-3330-7 | 50090333007 | 15 TABLET in 1 BOTTLE (50090-3330-7) | 15 tablet | 2018-01-15 | 0000-00-00 | No | No | Current |