Sodium Polystyrene Sulfonate
- Product NDC
- 17856-0036
- 11-digit product format
- 178560036
- Labeler code
- 17856
- Product ID
- 17856-0036_6a72a6a0-8516-499c-bdd3-cdd53e5b246e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Polystyrene Sulfonate
- Dosage form
- POWDER
- Route
- ORAL; RECTAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA040905
- Marketing category
- ANDA
- Marketing start
- 2012-07-25
- Marketing end
- 0000-00-00
- Substance
- SODIUM POLYSTYRENE SULFONATE
- Active strength
- 1 g/g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0036-1 | Sodium Polystyrene Sulfonate | 15 g in 1 POUCH | POWDER | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0036 | SODIUM POLYSTYRENE SULFONATE POWDER [ATLANTIC BIOLOGICALS CORPS] | 2 | Legacy NDC, 1 package rows | 20160504_34fe6cd2-70f1-4ea3-adb7-a3e37defc886.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-0036-1 | 17856003601 | 15 g in 1 POUCH | 15 g | Historical |