PREDNISONE
- Product NDC
- 68071-2500
- 11-digit product format
- 680712500
- Labeler code
- 68071
- Product ID
- 68071-2500_c94abe88-4ac9-7129-e053-2a95a90af82b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2018-12-07
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 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 |
|---|
| 68071-2500 | PREDNISONE TABLET [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC | 20210812_c94abe81-e32d-2b5a-e053-2995a90a099e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2500-1 | 68071250001 | 100 TABLET in 1 BOTTLE (68071-2500-1) | 100 tablet | 2021-08-11 | 0000-00-00 | No | No | Current |