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