Prednisone
- Product NDC
- 68788-7637
- 11-digit product format
- 687887637
- Labeler code
- 68788
- Product ID
- 68788-7637_ee4ac4d6-2b40-4ecf-810b-5fde5fe55fa6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 2020-06-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7637-1 | 68788763701 | 10 TABLET in 1 BOTTLE (68788-7637-1) | 10 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7637-2 | 68788763702 | 20 TABLET in 1 BOTTLE (68788-7637-2) | 20 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7637-3 | 68788763703 | 30 TABLET in 1 BOTTLE (68788-7637-3) | 30 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7637-4 | 68788763704 | 40 TABLET in 1 BOTTLE (68788-7637-4) | 40 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7637-6 | 68788763706 | 15 TABLET in 1 BOTTLE (68788-7637-6) | 15 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7637-7 | 68788763707 | 12 TABLET in 1 BOTTLE (68788-7637-7) | 12 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7637-8 | 68788763708 | 21 TABLET in 1 BOTTLE (68788-7637-8) | 21 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |
| 68788-7637-9 | 68788763709 | 90 TABLET in 1 BOTTLE (68788-7637-9) | 90 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |