multrys

Generic: trace elements injection 4

Labeler: american regent, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name multrys
Generic Name trace elements injection 4
Labeler american regent, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

cupric sulfate 150 ug/mL, manganese sulfate 8.22 ug/mL, selenious acid 9.8 ug/mL, zinc sulfate 2470 ug/mL

Manufacturer
American Regent, Inc.

Identifiers & Regulatory

Product NDC 0517-9302
Product ID 0517-9302_5c07b457-1143-440c-9975-90c16852a103
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA209376
Listing Expiration 2026-12-31
Marketing Start 2021-09-01

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe] magnetic resonance contrast activity [moa] paramagnetic contrast agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05179302
Hyphenated Format 0517-9302

Supplemental Identifiers

RxCUI
2568573 2568579
UPC
0305178201250
UNII
LRX7AJ16DT W00LYS4T26 F6A27P4Q4R 89DS0H96TB

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name multrys (source: ndc)
Generic Name trace elements injection 4 (source: ndc)
Application Number NDA209376 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 150 ug/mL
  • 8.22 ug/mL
  • 9.8 ug/mL
  • 2470 ug/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9302-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-9302-01)
source: ndc

Packages (1)

0517-9302-25 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9302-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-9302-01)

Ingredients (4)

cupric sulfate (150 ug/mL) manganese sulfate (8.22 ug/mL) selenious acid (9.8 ug/mL) zinc sulfate (2470 ug/mL)

Linked Drug Pages (1)

Multrys ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5c07b457-1143-440c-9975-90c16852a103", "openfda": {"upc": ["0305178201250"], "unii": ["LRX7AJ16DT", "W00LYS4T26", "F6A27P4Q4R", "89DS0H96TB"], "rxcui": ["2568573", "2568579"], "spl_set_id": ["995f1efa-aca0-4b6c-9099-f8e757c2133a"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9302-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (0517-9302-01)", "package_ndc": "0517-9302-25", "marketing_start_date": "20210901"}], "brand_name": "Multrys", "product_id": "0517-9302_5c07b457-1143-440c-9975-90c16852a103", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Magnetic Resonance Contrast Activity [MoA]", "Paramagnetic Contrast Agent [EPC]"], "product_ndc": "0517-9302", "generic_name": "Trace Elements Injection 4", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Multrys", "active_ingredients": [{"name": "CUPRIC SULFATE", "strength": "150 ug/mL"}, {"name": "MANGANESE SULFATE", "strength": "8.22 ug/mL"}, {"name": "SELENIOUS ACID", "strength": "9.8 ug/mL"}, {"name": "ZINC SULFATE", "strength": "2470 ug/mL"}], "application_number": "NDA209376", "marketing_category": "NDA", "marketing_start_date": "20210901", "listing_expiration_date": "20261231"}