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Sodium Polystyrene Sulfonate
Sodium Polystyrene Sulfonate - 42808-500-16 - (Sodium Polystyrene Sulfonate)
Drug Information of Sodium Polystyrene Sulfonate
| Product NDC: | 42808-500 |
| Proprietary Name: | Sodium Polystyrene Sulfonate |
| Non Proprietary Name: | Sodium Polystyrene Sulfonate |
| Active Ingredient(s): | 4.1 meq/g & nbsp; Sodium Polystyrene Sulfonate |
| Administration Route(s): | ORAL; RECTAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Polystyrene Sulfonate
| Product NDC: | 42808-500 |
| Labeler Name: | Exact-Rx, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040547 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120401 |
Package Information of Sodium Polystyrene Sulfonate
| Package NDC: | 42808-500-16 |
| Package Description: | 453.6 g in 1 JAR (42808-500-16) |
NDC Information of Sodium Polystyrene Sulfonate
| NDC Code | 42808-500-16 |
| Proprietary Name | Sodium Polystyrene Sulfonate |
| Package Description | 453.6 g in 1 JAR (42808-500-16) |
| Product NDC | 42808-500 |
| 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 | 20120401 |
| Marketing Category Name | ANDA |
| Labeler Name | Exact-Rx, Inc. |
| Substance Name | SODIUM POLYSTYRENE SULFONATE |
| Strength Number | 4.1 |
| Strength Unit | meq/g |
| Pharmaceutical Classes |
