Home NDC 0517-6202 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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0517-6202-25 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0517-6202-25 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 0517-6202-25 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 0517-6202-25 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 0517-6202-25 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 0517-6202-25 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 0517-6202-25 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 0517-6202-25 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 0517-6202-25 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 0517-6202-25 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 0517-6202-25 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 0517-6202-25 557ba5c1ecfa…9c80585c8c6e…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CHROMIC CHLORIDE ACTIVE INGREDIENT KB1PCR9DMW MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 CUPRIC SULFATE ACTIVE INGREDIENT LRX7AJ16DT MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 MANGANESE SULFATE ACTIVE INGREDIENT W00LYS4T26 MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 ZINC SULFATE HEPTAHYDRATE ACTIVE INGREDIENT N57JI2K7WP MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 CHROMIC CATION ACTIVE MOIETY X1N4508KF1 MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 CUPRIC CATION ACTIVE MOIETY 8CBV67279L MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 MANGANESE CATION (2+) ACTIVE MOIETY H6EP7W5457 MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 ZINC CATION ACTIVE MOIETY 13S1S8SF37 MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 SULFURIC ACID INACTIVE INGREDIENT O40UQP6WCF MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3 WATER INACTIVE INGREDIENT 059QF0KO0R MULTITRACE-4 NEONATAL (TRACE ELEMENTS 4) INJECTION, SOLUTION [AMERICAN REGENT, INC.] 3
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