Prednisone
- Product NDC
- 58118-5442
- 11-digit product format
- 581185442
- Labeler code
- 58118
- Product ID
- 58118-5442_b0269539-707a-3111-e053-2995a90ad956
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA085162
- Marketing category
- ANDA
- Marketing start
- 1987-11-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58118-5442 | PREDNISONE TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 6 | Legacy NDC | 20200926_87eb5466-b9a2-46f2-8f34-92837bac60ef.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-5442-8 | 58118544208 | 30 TABLET in 1 BLISTER PACK (58118-5442-8) | 30 tablet | 2017-01-24 | 0000-00-00 | No | No | Current |