PredniSONE
- Product NDC
- 68071-2578
- 11-digit product format
- 680712578
- Labeler code
- 68071
- Product ID
- 68071-2578_d12bf294-3bc7-420c-e053-2a95a90a61a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA080352
- Marketing category
- ANDA
- Marketing start
- 1972-04-21
- 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 |
|---|
| 68071-2578-1 | PredniSONE | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2578 | PREDNISONE TABLET [NUCARE PHARMACEUTICALS,INC.] | 3 | Legacy NDC, 1 package rows | 20230718_d12bf294-3bc9-420c-e053-2a95a90a61a3.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 |
|---|
| 68071-2578-1 | 68071257801 | 100 TABLET in 1 BOTTLE, PLASTIC (68071-2578-1) | 100 tablet | 2021-11-19 | 0000-00-00 | No | No | Current |