Prednisolone
- Product NDC
- 68788-9096
- 11-digit product format
- 687889096
- Labeler code
- 68788
- Product ID
- 68788-9096_1ab71a3c-8211-4a90-ac24-2eb8f96f8f2a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc
- Application
- ANDA040401
- Marketing category
- ANDA
- Marketing start
- 2003-02-27
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE
- Active strength
- 15 mg/5mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 68788-9096-2 | 68788909602 | 240 mL in 1 BOTTLE (68788-9096-2) | 240 ml | 2017-11-30 | 0000-00-00 | No | No | Current |
| 68788-9096-4 | 68788909604 | 1 BOTTLE in 1 CARTON (68788-9096-4) > 480 mL in 1 BOTTLE | 1 bottle | 2011-08-12 | 0000-00-00 | No | No | Current |