SODIUM POLYSTYRENE SULFONATE
- Product NDC
- 71335-2855
- 11-digit product format
- 713352855
- Labeler code
- 71335
- Product ID
- 71335-2855_d5a2166e-4e28-446e-a018-b1e3c4732bf0
- 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 |
|---|
| 71335-2855-1 | SODIUM POLYSTYRENE SULFONATE | 15 g in 1 BOTTLE | POWDER, FOR SUSPENSION | 15 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2855-1 | 71335285501 | 15 g in 1 BOTTLE (71335-2855-1) | 15 g | 2025-10-21 | No | No | Current |