Multitrace -4

Product NDC
0517-7201
11-digit product format
005177201
Labeler code
0517
Product ID
0517-7201_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
1993-12-07
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
Magnetic Resonance Contrast Activity [MoA],Paramagnetic Contrast Agent [EPC],Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE]
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
0517-7201-25ML - Milliliter0517-7201e3dfa97c-b6cd-4f21-8d49-414d4b4a538212014-09-03