PredniSONE
- Product NDC
- 67296-0247
- 11-digit product format
- 672960247
- Labeler code
- 67296
- Product ID
- 67296-0247_d5fbea2f-f360-900f-e053-2995a90a3887
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA087342
- Marketing category
- ANDA
- Marketing start
- 2003-02-13
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0247 | PREDNISONE TABLET [REDPHARM DRUG, INC.] | 5 | Legacy NDC, 5 package rows | 20240626_42897c99-311e-55bf-e054-00144ff8d46c.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 |
|---|
| 67296-0247-1 | 67296024701 | 10 TABLET in 1 BOTTLE (67296-0247-1) | 10 tablet | 2003-02-13 | 0000-00-00 | No | No | Current |
| 67296-0247-2 | 67296024702 | 15 TABLET in 1 BOTTLE (67296-0247-2) | 15 tablet | 2003-02-13 | 0000-00-00 | No | No | Current |
| 67296-0247-3 | 67296024703 | 20 TABLET in 1 BOTTLE (67296-0247-3) | 20 tablet | 2003-02-13 | 0000-00-00 | No | No | Current |
| 67296-0247-5 | 67296024705 | 5 TABLET in 1 BOTTLE (67296-0247-5) | 5 tablet | 2003-02-13 | 0000-00-00 | No | No | Current |
| 67296-0247-6 | 67296024706 | 30 TABLET in 1 BOTTLE (67296-0247-6) | 30 tablet | 2003-02-13 | 0000-00-00 | No | No | Current |