Kionex
- Product NDC
- 0574-2002
- 11-digit product format
- 005742002
- Labeler code
- 0574
- Product ID
- 0574-2002_88500449-5498-44f7-a97a-58e573bd833c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Polystyrene Sulfonate
- Dosage form
- SUSPENSION
- Route
- ORAL; RECTAL
- Labeler
- Paddock Laboratories, LLC
- Application
- ANDA040028
- Marketing category
- ANDA
- Marketing start
- 2008-12-30
- Marketing end
- 0000-00-00
- Substance
- SODIUM POLYSTYRENE SULFONATE
- Active strength
- 15 g/60mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record