prednisone
- Product NDC
- 68071-2696
- 11-digit product format
- 680712696
- Labeler code
- 68071
- Product ID
- 68071-2696_df371872-2984-7951-e053-2a95a90ad757
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA208412
- Marketing category
- ANDA
- Marketing start
- 2021-09-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68071-2696-4 | prednisone | 4 in 1 BOTTLE, PLASTIC | TABLET | 4 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2696 | PREDNISONE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 1 package rows | 20220518_df371872-2983-7951-e053-2a95a90ad757.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 |
|---|
| 68071-2696-4 | 68071269604 | 4 TABLET in 1 BOTTLE, PLASTIC (68071-2696-4) | 4 tablet | 2022-05-17 | 0000-00-00 | No | No | Current |