Prednisone
- Product NDC
- 42291-727
- 11-digit product format
- 422910727
- Labeler code
- 42291
- Product ID
- 42291-727_d5bf9b4d-804d-6196-e053-2a95a90a55bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2020-02-04
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42291-727 | PREDNISONE TABLET [AVKARE] | 4 | Legacy NDC | 20220117_9dc1f559-6799-8482-e053-2995a90a6d96.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-727-10 | 42291072710 | 1000 TABLET in 1 BOTTLE (42291-727-10) | 1000 tablet | 2020-02-04 | 0000-00-00 | No | No | Current |