SODIUM POLYSTYRENE SULFONATE
- Product NDC
- 63629-2390
- 11-digit product format
- 636292390
- Labeler code
- 63629
- Product ID
- 63629-2390_929068a8-cf62-468b-bc5c-b311d6b37f07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sodium polystyrene sulfonate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL; RECTAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204071
- Marketing category
- ANDA
- Marketing start
- 2017-01-24
- 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 |
|---|
| 63629-2390-1 | SODIUM POLYSTYRENE SULFONATE | 454 g in 1 JAR | POWDER, FOR SUSPENSION | 454 | | 104 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2390 | SODIUM POLYSTYRENE SULFONATE POWDER, FOR SUSPENSION [BRYANT RANCH PREPACK] | 104 | Current NDC, Legacy NDC, 1 package rows | 20250410_03a0b525-5e48-4e76-b1fa-700eab10d20a.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 |
|---|
| 63629-2390-1 | 63629239001 | 454 g in 1 JAR (63629-2390-1) | 454 g | 2021-02-22 | 0000-00-00 | No | No | Current |