Prednisone
- Product NDC
- 50436-1730
- 11-digit product format
- 504361730
- Labeler code
- 50436
- Product ID
- 50436-1730_9b9d01dc-4d46-4387-b906-c05b83817b34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2001-08-29
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50436-1730-5 | Prednisone | 21 in 1 BOTTLE | TABLET | 21 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-1730 | PREDNISONE TABLET PREDNISONE (PREDNISONE) TABLET [UNIT DOSE SERVICES] | 5 | Legacy NDC, 1 package rows | 20190514_1418d2f2-07d5-407a-81ca-380a5615b5b4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-1730-5 | 50436173005 | 21 in 1 BOTTLE | Historical |