PredniSONE
- Product NDC
- 35356-818
- 11-digit product format
- 353560818
- Labeler code
- 35356
- Product ID
- 35356-818_8e4a82dc-b85f-4f56-bbdd-ada970f752f5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA087342
- Marketing category
- ANDA
- Marketing start
- 2003-02-13
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 35356-818-10 | EA - Each | 35356-818 | a1106dbe-2a90-4210-adb9-f722a26e93ba | 1 | 2013-07-02 |
| 35356-818-15 | EA - Each | 35356-818 | c6d73bd3-72d2-4791-a719-8e91b087f57b | 1 | 2013-07-02 |
| 35356-818-18 | EA - Each | 35356-818 | 9900fd57-3832-4fae-abb3-7877a0556d33 | 1 | 2013-07-02 |
| 35356-818-20 | EA - Each | 35356-818 | f2fe24ca-27d1-4829-9c7f-79b746b80053 | 1 | 2013-07-02 |
| 35356-818-21 | EA - Each | 35356-818 | 1c22100c-7dee-40b3-b2a1-e25e9be916f7 | 1 | 2013-07-02 |
| 35356-818-30 | EA - Each | 35356-818 | 3ffe9f92-b5f4-4eda-9a3c-7711a9bf6a43 | 1 | 2013-07-02 |