PREDNISONE
- Product NDC
- 0527-2933
- 11-digit product format
- 005272933
- Labeler code
- 0527
- Product ID
- 0527-2933_dab611da-3264-4468-9f21-f880721bedf0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- Marketing end
- 2023-08-31
- Substance
- PREDNISONE
- Active strength
- 10 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 |
|---|
| 0527-2933-37 | 00527293337 | 100 TABLET in 1 BOTTLE, PLASTIC (0527-2933-37) | 100 tablet | 2018-12-04 | 0000-00-00 | No | No | Current |
| 0527-2933-41 | 00527293341 | 500 TABLET in 1 BOTTLE, PLASTIC (0527-2933-41) | 500 tablet | 2018-12-04 | 0000-00-00 | No | No | Current |