| Product NDC: | 0054-0379 |
| Proprietary Name: | Sodium Polystyrene Sulfonate |
| Non Proprietary Name: | Sodium Polystyrene Sulfonate |
| Active Ingredient(s): | 15 g/60mL & nbsp; Sodium Polystyrene Sulfonate |
| Administration Route(s): | ORAL; RECTAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0054-0379 |
| Labeler Name: | Roxane Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089049 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130617 |
| Package NDC: | 0054-0379-63 |
| Package Description: | 500 mL in 1 BOTTLE (0054-0379-63) |
| NDC Code | 0054-0379-63 |
| Proprietary Name | Sodium Polystyrene Sulfonate |
| Package Description | 500 mL in 1 BOTTLE (0054-0379-63) |
| Product NDC | 0054-0379 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Polystyrene Sulfonate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL; RECTAL |
| Start Marketing Date | 20130617 |
| Marketing Category Name | ANDA |
| Labeler Name | Roxane Laboratories, Inc. |
| Substance Name | SODIUM POLYSTYRENE SULFONATE |
| Strength Number | 15 |
| Strength Unit | g/60mL |
| Pharmaceutical Classes |