Sodium Polystyrene Sulfonate
- Product NDC
- 24658-760
- 11-digit product format
- 246580760
- Labeler code
- 24658
- Product ID
- 24658-760_ae811fb8-9a78-496f-b710-663bc678f8e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Polystyrene Sulfonate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- PuraCap Laboratories, LLC
- Application
- ANDA202333
- Marketing category
- ANDA
- Marketing start
- 2016-12-15
- Substance
- SODIUM POLYSTYRENE SULFONATE
- Active strength
- 4.1 meq/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sodium Polystyrene Sulfonate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM POLYSTYRENE SULFONATE | 4.1 meq/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1699G8679Z |
| Rxcui | 2101899 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24658-760-16 | Sodium Polystyrene Sulfonate | 453.6 g in 1 JAR | POWDER, FOR SUSPENSION | 453.6 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24658-760 | SODIUM POLYSTYRENE SULFONATE POWDER, FOR SUSPENSION [PURACAP LABORATORIES, LLC] | 5 | Current NDC, Legacy NDC, 1 package rows | 20221229_875d5288-db99-4440-8290-d9192bde6eee.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 |
|---|
| 24658-760-16 | 24658076016 | 453.6 g in 1 JAR (24658-760-16) | 453.6 g | 2016-12-15 | 0000-00-00 | No | No | Current |