Prednisone
- Product NDC
- 50090-3336
- 11-digit product format
- 500903336
- Labeler code
- 50090
- Product ID
- 50090-3336_2d4421d3-6e84-4e39-866d-c0d1cd407415
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3336 | PREDNISONE (PREDNISONE) TABLET [A-S MEDICATION SOLUTIONS] | 14 | Legacy NDC | 20231213_74102cc5-7a1a-4a0f-a07f-a4b0f86bcabf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3336-0 | 50090333600 | 8 TABLET in 1 BOTTLE (50090-3336-0) | 8 tablet | 2019-07-19 | 0000-00-00 | No | No | Current |
| 50090-3336-1 | 50090333601 | 10 TABLET in 1 BOTTLE (50090-3336-1) | 10 tablet | 2018-01-19 | 0000-00-00 | No | No | Current |
| 50090-3336-2 | 50090333602 | 21 TABLET in 1 BOTTLE (50090-3336-2) | 21 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |
| 50090-3336-3 | 50090333603 | 30 TABLET in 1 BOTTLE (50090-3336-3) | 30 tablet | 2018-02-16 | 0000-00-00 | No | No | Current |
| 50090-3336-5 | 50090333605 | 100 TABLET in 1 BOTTLE (50090-3336-5) | 100 tablet | 2022-07-20 | 0000-00-00 | No | No | Current |
| 50090-3336-9 | 50090333609 | 18 TABLET in 1 BOTTLE (50090-3336-9) | 18 tablet | 2022-07-20 | 0000-00-00 | No | No | Current |