Prednisone
- Product NDC
- 49999-028
- 11-digit product format
- 499990028
- Labeler code
- 49999
- Product ID
- 49999-028_0d8b6719-907e-49bb-ac00-c53f0b069377
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie medical DBA Quality Care Products LLC
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2010-08-11
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49999-028-21 | 49999002821 | 21 TABLET in 1 BOTTLE, PLASTIC (49999-028-21) | 21 tablet | 2014-09-05 | 0000-00-00 | No | No | Current |
| 49999-028-40 | 49999002840 | 40 TABLET in 1 BOTTLE, PLASTIC (49999-028-40) | 40 tablet | 2010-08-11 | 0000-00-00 | No | No | Current |
| 49999-028-60 | 49999002860 | 60 TABLET in 1 BOTTLE, PLASTIC (49999-028-60) | 60 tablet | 2010-08-11 | 0000-00-00 | No | No | Current |
| 49999-028-65 | 49999002865 | 21 TABLET in 1 BOTTLE, PLASTIC (49999-028-65) | 21 tablet | 2010-08-11 | 0000-00-00 | No | No | Current |