Package 31722-098-31

Brand: sodium sulfate, potassium sulfate and magnesium sulfate

Generic: sodium sulfate, potassium sulfate and magnesium sulfate
NDC Package

Package Facts

Identity

Package NDC 31722-098-31
Digits Only 3172209831
Product NDC 31722-098
Description

2 BOTTLE, PLASTIC in 1 CARTON (31722-098-31) / 177 mL in 1 BOTTLE, PLASTIC (31722-098-17)

Marketing

Marketing Status
Marketed Since 2024-10-18
Brand sodium sulfate, potassium sulfate and magnesium sulfate
Generic sodium sulfate, potassium sulfate and magnesium sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be51483-8976-9653-e063-6394a90ad0bc", "openfda": {"unii": ["DE08037SAB", "1K573LC5TV", "0YPR65R21J"], "rxcui": ["1120068"], "spl_set_id": ["315c377b-a634-45ea-9beb-c0f58dad551d"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (31722-098-31)  / 177 mL in 1 BOTTLE, PLASTIC (31722-098-17)", "package_ndc": "31722-098-31", "marketing_start_date": "20241018"}], "brand_name": "Sodium sulfate, potassium sulfate and magnesium sulfate", "product_id": "31722-098_2be51483-8976-9653-e063-6394a90ad0bc", "dosage_form": "SOLUTION", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "31722-098", "generic_name": "Sodium sulfate, potassium sulfate and magnesium sulfate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium sulfate, potassium sulfate and magnesium sulfate", "active_ingredients": [{"name": "MAGNESIUM SULFATE", "strength": "1.6 g/177mL"}, {"name": "POTASSIUM SULFATE", "strength": "3.13 g/177mL"}, {"name": "SODIUM SULFATE", "strength": "17.5 g/177mL"}], "application_number": "ANDA212903", "marketing_category": "ANDA", "marketing_start_date": "20241018", "listing_expiration_date": "20261231"}