Prednisone
- Product NDC
- 43063-644
- 11-digit product format
- 430630644
- Labeler code
- 43063
- Product ID
- 43063-644_7d397269-7926-63f5-e053-2991aa0adee0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA088832
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- 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 |
|---|---|---|---|---|---|
| 43063-644-10 | EA - Each | 43063-644 | 6af092ca-2cf7-4400-ad8f-0698345080a5 | 1 | 2016-03-04 |
| 43063-644-15 | EA - Each | 43063-644 | 7dee0d2f-294d-4857-ad0c-c4ed6e6a13cc | 1 | 2016-05-16 |
| 43063-644-20 | EA - Each | 43063-644 | 149d9ea4-1183-47af-a20a-62b705f9fce4 | 1 | 2016-03-04 |
| 43063-644-21 | EA - Each | 43063-644 | 0ca9bd3e-1563-40e0-9632-74798f1e911e | 1 | 2016-03-04 |
| 43063-644-30 | EA - Each | 43063-644 | 3afb437f-028b-4a69-887f-afed266d7ff9 | 1 | 2016-03-04 |
| 43063-644-40 | EA - Each | 43063-644 | 18ae6818-fe3e-4cf4-b318-24d28d013e60 | 1 | 2016-03-04 |
| 43063-644-42 | EA - Each | 43063-644 | fa09ca58-5917-4960-a031-1aba935138bd | 1 | 2016-03-04 |
| 43063-644-50 | EA - Each | 43063-644 | ee49b25f-ae09-4460-ab78-3edb4b7cb33d | 1 | 2016-04-04 |