Sodium Polystyrene Sulfonate
- Product NDC
- 50488-5001
- 11-digit product format
- 504885001
- Labeler code
- 50488
- Product ID
- 50488-5001_b49935c3-362e-4c68-a74e-f31e16226a9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Polystyrene Sulfonate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL; RECTAL
- Labeler
- Alexso, Inc
- Application
- ANDA090313
- Marketing category
- ANDA
- Marketing start
- 2017-02-07
- Marketing end
- 0000-00-00
- Substance
- SODIUM POLYSTYRENE SULFONATE
- Active strength
- 4 meq/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50488-5001-1 | 50488500101 | 453.6 g in 1 JAR (50488-5001-1) | 453.6 g | 2017-02-07 | 0000-00-00 | No | No | Current |