Multrys is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by American Regent, Inc.. The primary component is Zinc Sulfate; Cupric Sulfate; Manganese Sulfate; Selenious Acid.
Product ID | 0517-9302_d1c398ef-f162-49b3-89ff-59adff04ed27 |
NDC | 0517-9302 |
Product Type | Human Prescription Drug |
Proprietary Name | Multrys |
Generic Name | Trace Elements Injection 4 |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2021-09-01 |
Marketing Category | NDA / |
Application Number | NDA209376 |
Labeler Name | American Regent, Inc. |
Substance Name | ZINC SULFATE; CUPRIC SULFATE; MANGANESE SULFATE; SELENIOUS ACID |
Active Ingredient Strength | 2470 ug/mL; ug/mL; ug/mL; ug/mL |
Pharm Classes | Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2021-09-01 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
0517-9302 | Multrys | Trace Elements Injection 4 |
0517-9305 | Tralement | Trace Elements Injection 4 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MULTRYS 90579713 not registered Live/Pending |
American Regent, Inc. 2021-03-15 |
MULTRYS 88181166 not registered Live/Pending |
Luitpold Pharmaceuticals, Inc. 2018-11-05 |