Prednisone
- Product NDC
- 10544-913
- 11-digit product format
- 105440913
- Labeler code
- 10544
- Product ID
- 10544-913_74343126-7c09-4265-a3be-e67636278cb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2015-05-18
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10544-913-30 | Prednisone | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-913 | PREDNISONE (PREDNISONE) TABLET [BLENHEIM PHARMACAL, INC.] | 4 | Legacy NDC, 1 package rows | 20160418_dd933616-6988-4535-96b1-3c26d4432536.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-913-30 | 10544091330 | 30 in 1 BOTTLE | Historical |