Prednisone
- Product NDC
- 43063-911
- 11-digit product format
- 430630911
- Labeler code
- 43063
- Product ID
- 43063-911_e6d99d37-e309-52f0-e053-2995a90ae1ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2001-08-29
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-911 | PREDNISONE TABLET [PD-RX PHARMACEUTICALS, INC.] | 18 | Legacy NDC | 20240927_b452c4e5-91de-44fd-86c9-b4f7ab168d6f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-911-21 | 43063091121 | 21 TABLET in 1 BOTTLE, PLASTIC (43063-911-21) | 21 tablet | 2018-12-06 | 0000-00-00 | No | No | Current |