multitrace -4 pediatric

Generic: trace elements 4

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

Drug Facts

Product Profile

Brand Name multitrace -4 pediatric
Generic Name trace elements 4
Labeler american regent, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

chromic chloride 5.12 ug/mL, cupric sulfate .4 mg/mL, manganese sulfate 77 ug/mL, zinc sulfate heptahydrate 4.39 mg/mL

Manufacturer
American Regent, Inc.

Identifiers & Regulatory

Product NDC 0517-9203
Product ID 0517-9203_8e5be3e5-1916-4d19-87ab-e2092f5d4c5a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 1993-12-09

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 05179203
Hyphenated Format 0517-9203

Supplemental Identifiers

RxCUI
1293464 1293466
UPC
0305179203253
UNII
KB1PCR9DMW LRX7AJ16DT W00LYS4T26 N57JI2K7WP

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 multitrace -4 pediatric (source: ndc)
Generic Name trace elements 4 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5.12 ug/mL
  • .4 mg/mL
  • 77 ug/mL
  • 4.39 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9203-25) / 3 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

0517-9203-25 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9203-25) / 3 mL in 1 VIAL, SINGLE-DOSE

Ingredients (4)

chromic chloride (5.12 ug/mL) cupric sulfate (.4 mg/mL) manganese sulfate (77 ug/mL) zinc sulfate heptahydrate (4.39 mg/mL)

Linked Drug Pages (1)

Multitrace -4 Pediatric ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "8e5be3e5-1916-4d19-87ab-e2092f5d4c5a", "openfda": {"upc": ["0305179203253"], "unii": ["KB1PCR9DMW", "LRX7AJ16DT", "W00LYS4T26", "N57JI2K7WP"], "rxcui": ["1293464", "1293466"], "spl_set_id": ["5ee6a685-3c35-467b-8d4d-79efdd0bfa8e"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0517-9203-25)  / 3 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0517-9203-25", "marketing_start_date": "19931209"}], "brand_name": "Multitrace -4 Pediatric", "product_id": "0517-9203_8e5be3e5-1916-4d19-87ab-e2092f5d4c5a", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Magnetic Resonance Contrast Activity [MoA]", "Paramagnetic Contrast Agent [EPC]"], "product_ndc": "0517-9203", "generic_name": "Trace Elements 4", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Multitrace -4 Pediatric", "active_ingredients": [{"name": "CHROMIC CHLORIDE", "strength": "5.12 ug/mL"}, {"name": "CUPRIC SULFATE", "strength": ".4 mg/mL"}, {"name": "MANGANESE SULFATE", "strength": "77 ug/mL"}, {"name": "ZINC SULFATE HEPTAHYDRATE", "strength": "4.39 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19931209", "listing_expiration_date": "20261231"}