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Kionex
Kionex - 0574-2004-16 - (SODIUM POLYSTYRENE SULFONATE)
Drug Information of Kionex
| Product NDC: | 0574-2004 |
| Proprietary Name: | Kionex |
| 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 Kionex
| Product NDC: | 0574-2004 |
| Labeler Name: | Paddock Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040029 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980201 |
Package Information of Kionex
| Package NDC: | 0574-2004-16 |
| Package Description: | 454 g in 1 BOTTLE, PLASTIC (0574-2004-16) |
NDC Information of Kionex
| NDC Code | 0574-2004-16 |
| Proprietary Name | Kionex |
| Package Description | 454 g in 1 BOTTLE, PLASTIC (0574-2004-16) |
| Product NDC | 0574-2004 |
| 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 | 19980201 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, LLC |
| Substance Name | SODIUM POLYSTYRENE SULFONATE |
| Strength Number | 4.1 |
| Strength Unit | meq/g |
| Pharmaceutical Classes |
