Sodium Polystyrene Sulfonate
- Product NDC
- 70166-712
- 11-digit product format
- 701660712
- Labeler code
- 70166
- Product ID
- 70166-712_95827067-604e-d269-e053-2a95a90ab352
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Polystyrene Sulfonate
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL; RECTAL
- Labeler
- LOHXA
- 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
- 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 |
|---|
| 70166-712-10 | Sodium Polystyrene Sulfonate | 10 in 1 CELLO PACK | POWDER, FOR SUSPENSION | 10 | | 1 |
| 70166-712-10 | Sodium Polystyrene Sulfonate | 15 g in 1 BOTTLE | POWDER, FOR SUSPENSION | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70166-712 | SODIUM POLYSTYRENE SULFONATE POWDER, FOR SUSPENSION [LOHXA] | 1 | Legacy NDC, 2 package rows | 20191023_806b330b-6564-41c9-a87c-2d68a42e696a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 70166-712-10 | 70166071210 | 10 in 1 CELLO PACK | Historical |