Prednisone
- Product NDC
- 51655-208
- 11-digit product format
- 516550208
- Labeler code
- 51655
- Product ID
- 51655-208_c16e2c01-6175-9fff-e053-2995a90a2c40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NORTHWIND PHARMACEUTICALS
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2021-04-30
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 51655-208 | PREDNISONE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 5 | Legacy NDC | 20240709_c16e3020-c0bd-8f18-e053-2a95a90aa303.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51655-208-20 | 51655020820 | 20 TABLET in 1 BOTTLE, PLASTIC (51655-208-20) | 20 tablet | 2021-04-30 | 0000-00-00 | No | No | Current |