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Kionex
Kionex - 0574-2002-16 - (Sodium Polystyrene Sulfonate)
Drug Information of Kionex
| Product NDC: | 0574-2002 |
| Proprietary Name: | Kionex |
| 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) |
Labeler Information of Kionex
| Product NDC: | 0574-2002 |
| Labeler Name: | Paddock Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040028 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081230 |
Package Information of Kionex
| Package NDC: | 0574-2002-16 |
| Package Description: | 473 mL in 1 BOTTLE (0574-2002-16) |
NDC Information of Kionex
| NDC Code | 0574-2002-16 |
| Proprietary Name | Kionex |
| Package Description | 473 mL in 1 BOTTLE (0574-2002-16) |
| Product NDC | 0574-2002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Polystyrene Sulfonate |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL; RECTAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, LLC |
| Substance Name | SODIUM POLYSTYRENE SULFONATE |
| Strength Number | 15 |
| Strength Unit | g/60mL |
| Pharmaceutical Classes |
