PREDNISONE
- Product NDC
- 67296-1755
- 11-digit product format
- 672961755
- Labeler code
- 67296
- Product ID
- 67296-1755_d61f6438-c063-ed1f-e053-2995a90a5ff6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- 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#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1755-1 | PREDNISONE | 10 in 1 BOTTLE | TABLET | 10 | | 4 |
| 67296-1755-2 | PREDNISONE | 20 in 1 BOTTLE | TABLET | 20 | | 4 |
| 67296-1755-7 | PREDNISONE | 15 in 1 BOTTLE | TABLET | 15 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1755 | PREDNISONE TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 3 package rows | 20220123_a2f651f9-e1b9-3d2e-e053-2995a90a8896.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 |
|---|
| 67296-1755-1 | 67296175501 | 10 TABLET in 1 BOTTLE (67296-1755-1) | 10 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |
| 67296-1755-2 | 67296175502 | 20 TABLET in 1 BOTTLE (67296-1755-2) | 20 tablet | 2018-12-04 | 0000-00-00 | No | No | Current |
| 67296-1755-7 | 67296175507 | 15 TABLET in 1 BOTTLE (67296-1755-7) | 15 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |