Prednisone
- Product NDC
- 45865-670
- 11-digit product format
- 458650670
- Labeler code
- 45865
- Product ID
- 45865-670_9ab32ff5-b028-2d1f-e053-2a95a90a592b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2002-07-12
- 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 |
|---|
| 45865-670-40 | Prednisone | 40 in 1 BOTTLE, PLASTIC | TABLET | 40 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-670 | PREDNISONE TABLET [MEDSOURCE PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20191228_1f908a83-f50e-2f19-e054-00144ff88e88.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 |
|---|
| 45865-670-40 | 45865067040 | 40 TABLET in 1 BOTTLE, PLASTIC (45865-670-40) | 40 tablet | 2015-09-15 | 0000-00-00 | No | No | Current |