PHOXILLUM B22K4/0 is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Magnesium Chloride; Potassium Chloride; Sodium Bicarbonate; Sodium Chloride; Sodium Phosphate, Dibasic, Dihydrate.
Product ID | 24571-117_250f27ad-a700-4fd7-aaeb-7ca4211c17d8 |
NDC | 24571-117 |
Product Type | Human Prescription Drug |
Proprietary Name | PHOXILLUM B22K4/0 |
Generic Name | Magnesium Chloride, Sodium Chloride, Sodium Bicarbonate, Potassium Chloride And Sodium Phosphate Dibasic Dihydrate |
Dosage Form | Injection |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2015-01-13 |
Marketing Category | NDA / NDA |
Application Number | NDA207026 |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, DIHYDRATE |
Active Ingredient Strength | 3 g/L; g/L; g/L; g/L; g/L |
Pharm Classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], 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 Large Intestine Fluid/Electrolyte Absorption [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 Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2015-01-13 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA207026 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-13 |
Marketing Category | NDA |
Application Number | NDA207026 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-13 |
Marketing End Date | 2020-04-27 |
Ingredient | Strength |
---|---|
MAGNESIUM CHLORIDE | 3.05 g/L |
SPL SET ID: | 7f675fee-8940-4ece-bb0c-75ac79d8708c |
Manufacturer | |
UNII |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PHOXILLUM 86346945 4842319 Live/Registered |
GAMBRO LUNDIA AB 2014-07-24 |