Sodium Polystyrene Sulfonate
- Product NDC
- 17856-1136
- 11-digit product format
- 178561136
- Labeler code
- 17856
- Product ID
- 17856-1136_540c1dfc-9116-4402-83fa-2329deb9eb22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Polystyrene Sulfonate
- Dosage form
- POWDER
- Route
- ORAL; RECTAL
- Labeler
- ATLANTIC BIOLOGICALS CORP
- 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
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 17856-1136-1 | Sodium Polystyrene Sulfonate | 15 g in 1 POUCH | POWDER | 15 | | 4 |
| 17856-1136-2 | Sodium Polystyrene Sulfonate | 15 g in 1 CUP, UNIT-DOSE | POWDER | 15 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-1136 | SODIUM POLYSTYRENE SULFONATE POWDER [ATLANTIC BIOLOGICALS CORP] | 4 | Legacy NDC, 2 package rows | 20190926_e148d6d4-5abc-47c0-a365-8a14d03597a5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-1136-1 | 17856113601 | 15 g in 1 POUCH | 15 g | Historical |
| 17856-1136-2 | 17856113602 | 15 g in 1 CUP, UNIT-DOSE | 15 g | Historical |