Prednisolone Sodium Phosphate
- Product NDC
- 69101-410
- 11-digit product format
- 691010410
- Labeler code
- 69101
- Product ID
- 69101-410_b3b25567-9ede-d01d-e053-2a95a90ab80e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone Sodium Phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Burke Therapeutics
- Application
- ANDA078988
- Marketing category
- ANDA
- Marketing start
- 2018-06-12
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE SODIUM PHOSPHATE
- Active strength
- 20 mg/5mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 69101-410-01 | 69101041001 | 237 mL in 1 BOTTLE (69101-410-01) | 237 ml | 2018-06-12 | 0000-00-00 | No | No | Current |