Prednisolone Sodium Phosphate
- Product NDC
- 50383-040
- 11-digit product format
- 503830040
- Labeler code
- 50383
- Product ID
- 50383-040_81560ca8-9d04-4936-8779-64857bc376d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone Sodium Phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Akorn
- Application
- ANDA075183
- Marketing category
- ANDA
- Marketing start
- 2003-03-26
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE SODIUM PHOSPHATE
- Active strength
- 5 mg/5mL
- 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 |
|---|
| 50383-040-04 | 50383004004 | 120 mL in 1 BOTTLE (50383-040-04) | 120 ml | 2003-03-26 | 0000-00-00 | No | No | Current |