EXTRANEAL is a Intraperitoneal Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Icodextrin; Sodium Chloride; Sodium Lactate; Calcium Chloride; Magnesium Chloride.
Product ID | 0941-0679_3ab6f82d-5a8d-4eaf-82b8-15be5ec3a1df |
NDC | 0941-0679 |
Product Type | Human Prescription Drug |
Proprietary Name | EXTRANEAL |
Generic Name | Icodextrin, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride |
Dosage Form | Injection, Solution |
Route of Administration | INTRAPERITONEAL |
Marketing Start Date | 2002-12-20 |
Marketing Category | NDA / NDA |
Application Number | NDA021321 |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | ICODEXTRIN; SODIUM CHLORIDE; SODIUM LACTATE; CALCIUM CHLORIDE; MAGNESIUM CHLORIDE |
Active Ingredient Strength | 8 g/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],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],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] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2002-12-20 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2002-12-20 |
Marketing End Date | 2014-12-18 |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2002-12-20 |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-12-20 |
Marketing End Date | 2014-12-18 |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-12-20 |
Marketing End Date | 2014-12-18 |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2002-12-20 |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2002-12-20 |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2002-12-20 |
Marketing Category | NDA |
Application Number | NDA021321 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2002-12-20 |
Marketing End Date | 2014-12-18 |
Ingredient | Strength |
---|---|
ICODEXTRIN | 7.5 g/100mL |
SPL SET ID: | d5b85158-b0d6-4855-9d07-8d1b3ad9ab71 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EXTRANEAL 78566260 not registered Dead/Abandoned |
Baxter International Inc. 2005-02-13 |
EXTRANEAL 76221877 not registered Dead/Abandoned |
Baxter International Inc. 2001-03-09 |
EXTRANEAL 76221144 2843444 Live/Registered |
Baxter International Inc. 2001-03-08 |
EXTRANEAL 75265684 not registered Dead/Abandoned |
Baxter International Inc. 1997-03-28 |
EXTRANEAL 75250390 not registered Dead/Abandoned |
Baxter International Inc. 1997-03-03 |