Product NDC: | 46287-006 |
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: | 46287-006 |
Labeler Name: | Carolina Medical Products Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087859 |
Marketing Category: | ANDA |
Start Marketing Date: | 19830101 |
Package NDC: | 46287-006-60 |
Package Description: | 10 BOTTLE, UNIT-DOSE in 1 CARTON (46287-006-60) > 60 mL in 1 BOTTLE, UNIT-DOSE |
NDC Code | 46287-006-60 |
Proprietary Name | Sodium Polystyrene Sulfonate |
Package Description | 10 BOTTLE, UNIT-DOSE in 1 CARTON (46287-006-60) > 60 mL in 1 BOTTLE, UNIT-DOSE |
Product NDC | 46287-006 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sodium polystyrene sulfonate |
Dosage Form Name | SUSPENSION |
Route Name | ORAL; RECTAL |
Start Marketing Date | 19830101 |
Marketing Category Name | ANDA |
Labeler Name | Carolina Medical Products Company |
Substance Name | SODIUM POLYSTYRENE SULFONATE |
Strength Number | 15 |
Strength Unit | g/60mL |
Pharmaceutical Classes |