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: | 0054-0379-55 |
Package Description: | 1 BOTTLE in 1 CARTON (0054-0379-55) > 200 mL in 1 BOTTLE |
NDC Code | 0054-0379-55 |
Proprietary Name | Sodium Polystyrene Sulfonate |
Package Description | 1 BOTTLE in 1 CARTON (0054-0379-55) > 200 mL in 1 BOTTLE |
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 |