Multitrace-4 Neonatal
- Product NDC
- 0517-6202
- 11-digit product format
- 005176202
- Labeler code
- 0517
- Product ID
- 0517-6202_90d7ca6a-674a-4b17-80f6-8da79ab38bd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trace Elements 4
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- ZINC SULFATE HEPTAHYDRATE; CUPRIC SULFATE; MANGANESE SULFATE; CHROMIC CHLORIDE
- Active strength
- 7 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0517-6202-25 | 00517620225 | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6202-25) > 2 mL in 1 VIAL, SINGLE-DOSE | 1990-09-30 | 0000-00-00 | No | No | Current |