Prednisone
- Product NDC
- 50090-3335
- 11-digit product format
- 500903335
- Labeler code
- 50090
- Product ID
- 50090-3335_a03c8073-1ec5-41a8-9fba-4281f27f3839
- 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#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3335-0 | Prednisone | 21 in 1 BOTTLE | TABLET | 21 | | 22 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3335 | PREDNISONE (PREDNISONE) TABLET [A-S MEDICATION SOLUTIONS] | 19 | Legacy NDC, 1 package rows | 20240604_dc94273f-af06-4bd5-9ce3-ce0a0f36587b.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 |
|---|
| 50090-3335-0 | 50090333500 | 21 TABLET in 1 BOTTLE (50090-3335-0) | 21 tablet | 2018-01-17 | 0000-00-00 | No | No | Current |