SODIUM POLYSTYRENE SULFONATE
- Product NDC
- 63629-8849
- 11-digit product format
- 636298849
- Labeler code
- 63629
- Product ID
- 63629-8849_beecdb86-1fa6-4739-b976-b4227eb671da
- 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 |
|---|
| 63629-8849-1 | 63629884901 | 15 g in 1 BOTTLE (63629-8849-1) | 15 g | 2021-09-20 | No | No | Historical |