Prednisone
- Product NDC
- 43063-426
- 11-digit product format
- 430630426
- Labeler code
- 43063
- Product ID
- 43063-426_7d68485b-0717-445b-e053-2991aa0abe78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2002-07-12
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 43063-426-10 | EA - Each | 43063-426 | 202f7662-a439-40a9-bff9-58ff8cd43397 | 1 | 2013-06-04 |
| 43063-426-12 | EA - Each | 43063-426 | eef35eda-20b3-405a-b049-415d9d7ca22a | 1 | 2014-05-02 |
| 43063-426-20 | EA - Each | 43063-426 | 40e61381-9a67-4ad9-9151-db6751c70f85 | 1 | 2013-02-13 |
| 43063-426-21 | EA - Each | 43063-426 | ea15ee2f-6a12-4849-913f-991ae83b2df2 | 1 | 2013-02-13 |
| 43063-426-28 | EA - Each | 43063-426 | 135dae7b-bbe0-4e5a-8aad-940188d9b914 | 1 | 2016-07-19 |
| 43063-426-30 | EA - Each | 43063-426 | d60d536e-9a11-42dc-8042-6eccecc21ffa | 1 | 2013-02-13 |
| 43063-426-40 | EA - Each | 43063-426 | 67fd7ec0-dcfb-48b1-8236-eeaad6b78340 | 1 | 2013-02-13 |
| 43063-426-42 | EA - Each | 43063-426 | 3c891b7d-2870-48de-a1b0-3151a4baa306 | 1 | 2013-02-13 |
| 43063-426-50 | EA - Each | 43063-426 | ac6a2be4-4b6a-4083-80a8-cc88483ca1b0 | 1 | 2013-02-13 |
| 43063-426-60 | EA - Each | 43063-426 | b8d8bf84-f2d9-4234-aaeb-adb521982d30 | 1 | 2013-02-13 |