Prednisone
- Product NDC
- 51655-320
- 11-digit product format
- 516550320
- Labeler code
- 51655
- Product ID
- 51655-320_b9bb8a5e-0706-459f-917c-77e8fcacffa2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA088832
- Marketing category
- ANDA
- Marketing start
- 2014-04-29
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/201
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-320 | PREDNISONE TABLET [NORTHWIND PHARMACEUTICALS] | 4 | Legacy NDC | 20150122_2a994060-a358-4835-892b-0eb1f0806eb0.zip |
| 51655-320 | PREDNISONE TABLET [NORTHWIND PHARMACEUTICALS] | 1 | Legacy NDC | 20140501_c7acd116-7bda-4976-9f5f-cd5e7ddc0d02.zip |