Prednisone
- Product NDC
- 55695-014
- 11-digit product format
- 556950014
- Labeler code
- 55695
- Product ID
- 55695-014_2bd7831d-4626-1818-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2002-07-12
- 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
- 2018-12-31
- 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 |
|---|
| 55695-014-00 | Prednisone | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55695-014 | PREDNISONE TABLET [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] | 1 | Legacy NDC, 1 package rows | 20160311_2bd7831d-466e-1818-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55695-014-00 | 55695001400 | 100 in 1 BOTTLE, PLASTIC | Historical |