Multitrace-5
- Product NDC
- 0517-8201
- 11-digit product format
- 005178201
- Labeler code
- 0517
- Product ID
- 0517-8201_084307ad-f65d-4fbc-9177-6e26f664667f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trace Elements 5
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1993-12-17
- Marketing end
- 0000-00-00
- Substance
- ZINC SULFATE HEPTAHYDRATE; CUPRIC SULFATE; MANGANESE SULFATE; CHROMIC CHLORIDE; SELENIOUS ACID
- Active strength
- 22 mg/mL; mg/mL; mg/mL; ug/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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0517-8201-25 | 00517820125 | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-8201-25) > 1 mL in 1 VIAL, SINGLE-DOSE | 1993-12-17 | 0000-00-00 | No | No | Current |