Sodium Polystyrene Sulfonate
- Product NDC
- 63629-2031
- 11-digit product format
- 636292031
- Labeler code
- 63629
- Product ID
- 63629-2031_4dd2d177-1b29-4be7-a227-0c2dc3a55fee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Polystyrene Sulfonate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL; RECTAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2031 | SODIUM POLYSTYRENE SULFONATE POWDER, FOR SUSPENSION [BRYANT RANCH PREPACK] | 103 | Legacy NDC | 20230223_a9ed75ff-0adc-498e-b230-1d14f3eade64.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2031-1 | 63629203101 | 453.6 g in 1 JAR (63629-2031-1) | 453.6 g | 2022-03-08 | 0000-00-00 | No | No | Current |