Prednisone
- Product NDC
- 68071-2594
- 11-digit product format
- 680712594
- Labeler code
- 68071
- Product ID
- 68071-2594_d2bd9bd7-3f77-7a4b-e053-2995a90a9bfe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA080356
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-2594-1 | Prednisone | 21 in 1 BOTTLE | TABLET | 21 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2594 | PREDNISONE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 1 package rows | 20211212_d2bda01e-c8af-6e75-e053-2a95a90ab5a7.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 |
|---|
| 68071-2594-1 | 68071259401 | 21 TABLET in 1 BOTTLE (68071-2594-1) | 21 tablet | 2021-12-09 | 0000-00-00 | No | No | Current |