Prednisolone Sodium Phosphate
- Product NDC
- 71626-902
- 11-digit product format
- 716260902
- Labeler code
- 71626
- Product ID
- 71626-902_ea8466d1-19a4-4074-9659-f5858d2f6164
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone Sodium Phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Medstone Pharma LLC
- Application
- ANDA078988
- Marketing category
- ANDA
- Marketing start
- 2017-01-31
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71626-902-05 | Prednisolone Sodium Phosphate | 5 mL in 1 CUP, UNIT-DOSE | SOLUTION | 5 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71626-902 | PREDNISOLONE SODIUM PHOSPHATE SOLUTION [MEDSTONE PHARMA LLC] | 1 | Legacy NDC, 1 package rows | 20210310_2162943d-15a8-49bd-8717-f728a6808e03.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71626-902-05 | 71626090205 | 5 mL in 1 CUP, UNIT-DOSE (71626-902-05) | 5 ml | 2017-01-31 | 0000-00-00 | No | No | Current |