Prednisolone Sodium Phosphate
- Product NDC
- 67296-2134
- 11-digit product format
- 672962134
- Labeler code
- 67296
- Product ID
- 67296-2134_46aca408-309a-ee64-e063-6294a90a5f4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone Sodium Phosphate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA203559
- Marketing category
- ANDA
- Marketing start
- 2023-10-09
- Substance
- PREDNISOLONE SODIUM PHOSPHATE
- Active strength
- 15 mg/5mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Prednisolone Sodium Phosphate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PREDNISOLONE SODIUM PHOSPHATE | 15 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | IV021NXA9J |
| Rxcui | 283077 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-2134-6 | Prednisolone Sodium Phosphate | 60 mL in 1 BOTTLE, PLASTIC | SOLUTION | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-2134 | PREDNISOLONE SODIUM PHOSPHATE SOLUTION [REDPHARM DRUG] | 1 | Current NDC, 1 package rows | 20250410_3253b63b-0533-6cdc-e063-6294a90aa311.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2134-6 | 67296213406 | 60 mL in 1 BOTTLE, PLASTIC (67296-2134-6) | 60 ml | 2023-10-09 | No | No | Current |