| Product NDC: | 46287-012 |
| Proprietary Name: | Sodium Polystyrene Sulfonate |
| Non Proprietary Name: | Sodium Polystyrene Sulfonate |
| Active Ingredient(s): | 1 g/g & nbsp; Sodium Polystyrene Sulfonate |
| Administration Route(s): | ORAL; RECTAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 46287-012 |
| Labeler Name: | Carolina Medical Products Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089910 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19890119 |
| Package NDC: | 46287-012-16 |
| Package Description: | 454 g in 1 JAR (46287-012-16) |
| NDC Code | 46287-012-16 |
| Proprietary Name | Sodium Polystyrene Sulfonate |
| Package Description | 454 g in 1 JAR (46287-012-16) |
| Product NDC | 46287-012 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Polystyrene Sulfonate |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL; RECTAL |
| Start Marketing Date | 19890119 |
| Marketing Category Name | ANDA |
| Labeler Name | Carolina Medical Products Company |
| Substance Name | SODIUM POLYSTYRENE SULFONATE |
| Strength Number | 1 |
| Strength Unit | g/g |
| Pharmaceutical Classes |