sodium sulfate, potassium sulfate and magnesium sulfate
Generic: sodium sulfate, potassium sulfate and magnesium sulfate
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
sodium sulfate, potassium sulfate and magnesium sulfate
Generic Name
sodium sulfate, potassium sulfate and magnesium sulfate
Labeler
camber pharmaceuticals, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
magnesium sulfate 1.6 g/177mL, potassium sulfate 3.13 g/177mL, sodium sulfate 17.5 g/177mL
Manufacturer
Identifiers & Regulatory
Product NDC
31722-098
Product ID
31722-098_2be51483-8976-9653-e063-6394a90ad0bc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212903
Listing Expiration
2026-12-31
Marketing Start
2024-10-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722098
Hyphenated Format
31722-098
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sodium sulfate, potassium sulfate and magnesium sulfate (source: ndc)
Generic Name
sodium sulfate, potassium sulfate and magnesium sulfate (source: ndc)
Application Number
ANDA212903 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.6 g/177mL
- 3.13 g/177mL
- 17.5 g/177mL
Packaging
- 2 BOTTLE, PLASTIC in 1 CARTON (31722-098-31) / 177 mL in 1 BOTTLE, PLASTIC (31722-098-17)
Packages (1)
Ingredients (3)
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"}