TIS-U-SOL is a Irrigation Irrigant in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Sodium Chloride; Potassium Chloride; Magnesium Sulfate Heptahydrate; Sodium Phosphate, Dibasic, Heptahydrate; Potassium Phosphate, Monobasic.
Product ID | 0338-0190_9691bfc4-5e95-4b08-8227-f81f38bc5d66 |
NDC | 0338-0190 |
Product Type | Human Prescription Drug |
Proprietary Name | TIS-U-SOL |
Generic Name | Sodium Chloride, Potassium Chloride, Magnesium Sulfate, Sodium Phosphate, And Potassium Phosphate |
Dosage Form | Irrigant |
Route of Administration | IRRIGATION |
Marketing Start Date | 1982-02-19 |
Marketing Category | NDA / NDA |
Application Number | NDA018508 |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | SODIUM CHLORIDE; POTASSIUM CHLORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; POTASSIUM PHOSPHATE, MONOBASIC |
Active Ingredient Strength | 800 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL |
Pharm Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 1982-02-19 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA018508 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1982-02-19 |
Ingredient | Strength |
---|---|
SODIUM CHLORIDE | 800 mg/100mL |
SPL SET ID: | 9da4121f-d62d-4da4-8dfb-0494da16015f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TIS-U-SOL 72067113 0686832 Live/Registered |
BAXTER LABORATORIES, INC. 1959-02-05 |