Multrys
These highlights do not include all the information needed to use MULTRYS safely and effectively. See full prescribing information for MULTRYS
Approved
Approval ID
995f1efa-aca0-4b6c-9099-f8e757c2133a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 1, 2021
Manufacturers
FDA
American Regent, Inc.
DUNS: 002033710
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Trace Elements Injection 4
PRODUCT DETAILS
NDC Product Code0517-9302
Application NumberNDA209376
Marketing CategoryC73594
Route of AdministrationINTRAVENOUS
Effective DateJuly 9, 2021
Generic NameTrace Elements Injection 4
INGREDIENTS (5)
SELENIOUS ACIDActive
Quantity: 9.8 ug in 1 mL
Code: F6A27P4Q4R
Classification: ACTIB
ZINC SULFATEActive
Quantity: 2470 ug in 1 mL
Code: 89DS0H96TB
Classification: ACTIM
CUPRIC SULFATEActive
Quantity: 150 ug in 1 mL
Code: LRX7AJ16DT
Classification: ACTIM
MANGANESE SULFATEActive
Quantity: 8.22 ug in 1 mL
Code: W00LYS4T26
Classification: ACTIM
WATERInactive
Code: 059QF0KO0R
Classification: IACT