Prednisone
- Product NDC
- 71335-2153
- 11-digit product format
- 713352153
- Labeler code
- 71335
- Product ID
- 71335-2153_0fc6e657-8df4-4a3e-808f-abbf2fcce124
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040611
- Marketing category
- ANDA
- Marketing start
- 2005-06-06
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 1 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2153 | PREDNISONE TABLET [BRYANT RANCH PREPACK] | 101 | Legacy NDC | 20230608_e1f0600b-8e6c-4fe1-b687-0a34e6b9cab2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2153-1 | 71335215301 | 100 TABLET in 1 BOTTLE (71335-2153-1) | 100 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |
| 71335-2153-2 | 71335215302 | 30 TABLET in 1 BOTTLE (71335-2153-2) | 30 tablet | 2022-08-22 | 0000-00-00 | No | No | Current |