PREDNISONE
- Product NDC
- 68788-8108
- 11-digit product format
- 687888108
- Labeler code
- 68788
- Product ID
- 68788-8108_d079ebe1-1fb0-4b49-b56e-66f99d537bfd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2018-12-07
- Marketing end
- 2022-12-31
- Substance
- PREDNISONE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68788-8108-3 | 68788810803 | 30 TABLET in 1 BOTTLE (68788-8108-3) | 30 tablet | 2021-11-05 | 2022-12-31 | No | No | Current |