PREDNISONE
- Product NDC
- 0527-2930
- 11-digit product format
- 005272930
- Labeler code
- 0527
- Product ID
- 0527-2930_978ad77b-3f4d-4c14-b16e-5b78d81ca3bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA211496
- Marketing category
- ANDA
- Marketing start
- 2018-12-28
- Marketing end
- 2023-08-31
- Substance
- PREDNISONE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-2930-37 | 00527293037 | 100 TABLET in 1 BOTTLE (0527-2930-37) | 100 tablet | 2018-12-28 | 2023-08-31 | No | No | Current |
| 0527-2930-43 | 00527293043 | 1000 TABLET in 1 BOTTLE (0527-2930-43) | 1000 tablet | 2018-12-28 | 2023-08-31 | No | No | Current |