Prednisone
- Product NDC
- 0904-7127
- 11-digit product format
- 009047127
- Labeler code
- 0904
- Product ID
- 0904-7127_5d2181be-c5ac-4c11-b680-66f3710801c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2001-08-29
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7127 | PREDNISONE TABLET [MAJOR PHARMACEUTICALS] | 4 | Legacy NDC | 20250119_5d2181be-c5ac-4c11-b680-66f3710801c2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7127-61 | 00904712761 | 100 BLISTER PACK in 1 CARTON (0904-7127-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2001-08-29 | 0000-00-00 | No | No | Current |