SODIUM POLYSTYRENE SULFONATE
- Product NDC
- 72162-1230
- 11-digit product format
- 721621230
- Labeler code
- 72162
- Product ID
- 72162-1230_34f44991-fc66-a383-e063-6294a90a24cf
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 1699G8679Z | SODIUM POLYSTYRENE SULFONATE | 9080-79-9 | SODIUM POLYSTYRENE SULFONATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1230-2 | 72162123002 | 454 g in 1 JAR (72162-1230-2) | 454 g | 2023-09-13 | No | No | Historical |
| 72162-1230-7 | 72162123007 | 15 g in 1 BOTTLE (72162-1230-7) | 15 g | 2023-09-13 | No | No | Historical |