Prednisone
- Product NDC
- 68788-7692
- 11-digit product format
- 687887692
- Labeler code
- 68788
- Product ID
- 68788-7692_7f948d34-68f9-4dc6-a5a6-356265af4c61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA080356
- Marketing category
- ANDA
- Marketing start
- 2020-04-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7692-1 | 68788769201 | 10 TABLET in 1 BOTTLE (68788-7692-1) | 10 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |
| 68788-7692-2 | 68788769202 | 20 TABLET in 1 BOTTLE (68788-7692-2) | 20 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |
| 68788-7692-3 | 68788769203 | 30 TABLET in 1 BOTTLE (68788-7692-3) | 30 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |
| 68788-7692-4 | 68788769204 | 40 TABLET in 1 BOTTLE (68788-7692-4) | 40 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |
| 68788-7692-8 | 68788769208 | 21 TABLET in 1 BOTTLE (68788-7692-8) | 21 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |
| 68788-7692-9 | 68788769209 | 90 TABLET in 1 BOTTLE (68788-7692-9) | 90 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |