Prednisone
- Product NDC
- 50090-1991
- 11-digit product format
- 500901991
- Labeler code
- 50090
- Product ID
- 50090-1991_eddf038b-11cf-4dc9-89c7-8633ca69b9fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040392
- Marketing category
- ANDA
- Marketing start
- 2003-02-12
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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 |
|---|
| 50090-1991-0 | Prednisone | 21 in 1 BOTTLE | TABLET | 21 | | 21 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1991 | PREDNISONE TABLET [A-S MEDICATION SOLUTIONS] | 21 | Legacy NDC, 1 package rows | 20210808_5e802202-77dd-4d47-abe9-3cb668fa630d.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 |
|---|
| 50090-1991-0 | 50090199100 | 21 TABLET in 1 BOTTLE (50090-1991-0) | 21 tablet | 2015-09-17 | 0000-00-00 | No | No | Current |