Prednisolone Sodium Phosphate
- Product NDC
- 0121-0902
- 11-digit product format
- 001210902
- Labeler code
- 0121
- Product ID
- 0121-0902_c2c5fb34-8e7e-4954-e053-2a95a90ad0ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone Sodium Phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA075988
- Marketing category
- ANDA
- Marketing start
- 2004-05-25
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE SODIUM PHOSPHATE
- Active strength
- 5 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-0902-04 | 00121090204 | 120 mL in 1 BOTTLE (0121-0902-04) | 120 ml | 2021-05-10 | 0000-00-00 | No | No | Current |