Package 51672-4170-5

{"route": ["ORAL"], "spl_id": "494f52da-8ae6-6ec4-e063-6294a90a73a6", "openfda": {"upc": ["0351672417055"], "unii": ["DE08037SAB", "1K573LC5TV", "36KCS0R750"], "rxcui": ["1001689", "1120068"], "spl_set_id": ["4adeeb11-0f3a-47d8-a664-376df50b05f2"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (51672-4170-5)  / 177 mL in 1 BOTTLE", "package_ndc": "51672-4170-5", "marketing_start_date": "20240327"}], "brand_name": "Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit", "product_id": "51672-4170_494f52da-8ae6-6ec4-e063-6294a90a73a6", "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": "51672-4170", "generic_name": "sodium sulfate anhydrous, potassium sulfate, and magnesium sulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit", "active_ingredients": [{"name": "MAGNESIUM SULFATE, UNSPECIFIED FORM", "strength": "1.6 g/177mL"}, {"name": "POTASSIUM SULFATE", "strength": "3.13 g/177mL"}, {"name": "SODIUM SULFATE ANHYDROUS", "strength": "17.5 g/177mL"}], "application_number": "ANDA206431", "marketing_category": "ANDA", "marketing_start_date": "20240327", "listing_expiration_date": "20271231"}