Prednisone
- Product NDC
- 67296-1032
- 11-digit product format
- 672961032
- Labeler code
- 67296
- Product ID
- 67296-1032_9c9b6115-2a65-08ed-e053-2995a90a9239
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA088832
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- 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
- 2021-12-31
- 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 |
|---|
| 67296-1032-1 | Prednisone | 10 in 1 BOTTLE | TABLET | 10 | | 2 |
| 67296-1032-3 | Prednisone | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 67296-1032-4 | Prednisone | 40 in 1 BOTTLE | TABLET | 40 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1032 | PREDNISONE TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 3 package rows | 20200121_4e2cd6ec-edab-1f45-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 |
|---|
| 67296-1032-1 | 67296103201 | 10 TABLET in 1 BOTTLE (67296-1032-1) | 10 tablet | 2009-08-03 | 0000-00-00 | No | No | Current |
| 67296-1032-3 | 67296103203 | 30 TABLET in 1 BOTTLE (67296-1032-3) | 30 tablet | 2009-08-03 | 0000-00-00 | No | No | Current |
| 67296-1032-4 | 67296103204 | 40 TABLET in 1 BOTTLE (67296-1032-4) | 40 tablet | 2009-08-03 | 0000-00-00 | No | No | Current |