Multitrace -4

Product NDC
0517-7210
11-digit product format
005177210
Labeler code
0517
Product ID
0517-7210_1e30d2c3-d92d-474f-93f0-c335824bc3e3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trace Elements 4
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Labeler
American Regent, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1993-11-29
Marketing end
0000-00-00
Substance
ZINC SULFATE HEPTAHYDRATE; CUPRIC SULFATE; MANGANESE SULFATE; CHROMIC CHLORIDE
Active strength
22 mg/mL; mg/mL; mg/mL; ug/mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0517-7210-25ML - Milliliter0517-7210520b7c59-11bf-42ce-a4f7-d176bb66d11412014-09-03