PredniSONE
- Product NDC
- 51407-358
- 11-digit product format
- 514070358
- Labeler code
- 51407
- Product ID
- 51407-358_eb659bc5-4f12-320a-e053-2995a90af699
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA084122
- Marketing category
- ANDA
- Marketing start
- 1982-01-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-358 | PREDNISONE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.] | 10 | Legacy NDC | 20250126_a745b3fd-8deb-9d48-e053-2995a90ab7f4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-358-01 | 51407035801 | 100 TABLET in 1 BOTTLE, PLASTIC (51407-358-01) | 100 tablet | 2020-02-26 | 0000-00-00 | No | No | Current |
| 51407-358-05 | 51407035805 | 500 TABLET in 1 BOTTLE, PLASTIC (51407-358-05) | 500 tablet | 2020-02-26 | 0000-00-00 | No | No | Current |