MedPath

Chromic chloride

Generic Name
Chromic chloride
Brand Names
Multitrace-4, Multitrace-5
Drug Type
Small Molecule
Chemical Formula
Cl3Cr
CAS Number
10025-73-7
Unique Ingredient Identifier
Z310X5O5RP

Overview

Chromic chloride, for injection, is a sterile, nonpyrogenic solution intended for use as an additive to solutions for Total Parenteral Nutrition (TPN).

Indication

For use as a supplement to intravenous solutions given for total parenteral nutrition (TPN).

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
American Regent, Inc.
0517-8510
INTRAVENOUS
20.5 ug in 1 mL
4/25/2019
Hospira, Inc.
0409-4093
INTRAVENOUS
4 ug in 1 mL
6/28/2021
HF Acquisition Co LLC, DBA HealthFirst
51662-1415
INTRAVENOUS
4 ug in 1 mL
2/22/2020
American Regent, Inc.
0517-9203
INTRAVENOUS
5.12 ug in 1 mL
4/25/2019
Hospira, Inc.
0409-4093
INTRAVENOUS
4 ug in 1 mL
6/28/2021

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
ADDAVEN CONCENTRATE FOR SOLUTION FOR INFUSION
SIN15302P
INFUSION, SOLUTION CONCENTRATE
5.33 mcg/ml
7/24/2017

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
MaxN-Fuze Multivitamins
288444
Max Health & Living Australia Pty Ltd
Medicine
A
5/1/2017
NUTRA-LIFE BILBERRY 10,000 PLUS
310442
Medicine
A
10/17/2018
USANA HealthPak
350153
Medicine
A
11/30/2020
My Vit Women’s Breastfeeding and Pregnancy
349252
Medicine
A
11/23/2020
Quality Health Australia Daily Multi
404880
Pharmacare Laboratories Pty Ltd
Medicine
A
2/15/2023
ElementAll Diet
447331
Medicine
A
5/1/2024
Natal Care
395834
Medicine
A
9/12/2022
Adult Vita Gummies Women's Multivitamin
461189
Pharmacare Laboratories Pty Ltd
Medicine
A
8/29/2024
FBX Platinum Berberine +
451253
Medicine
A
6/6/2024
WelleCo Australia The PMS Elixir
380270
Medicine
A
12/6/2021

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
TRACE ELEMENTS SOLUTION INJ
david bull laboratories (pty) ltd.
00861979
Solution - Intravenous
.102 MG / 5 ML
12/31/1991
COMPLETE FORMULA FOR ADULTS TAB
ksl pharmaceuticals
02047527
Tablet - Oral
25 MCG / TAB
12/31/1995
PALM SPRINGS MULTVIT AND MIN TAB
l & s research corporation
01945580
Tablet - Oral
8.4 MCG / TAB
12/31/1993
TRACE ELEMENTS INJECTION USP
00569046
Solution - Intravenous
6 MCG / ML
12/31/1983
PRENATAL VITAMIN AND MINERAL SUPPLEMENT TAB
ksl pharmaceuticals
01995839
Tablet - Oral
25 MCG / TAB
12/31/1993
FUSION ACTIVATOR FORMULA TAB
l & s research corporation
01961144
Tablet - Oral
8 MCG / TAB
12/31/1993
TRACE ELEMENTS FOR INJECTION - LIQ IV
faulding (canada) inc.
02137143
Liquid - Intravenous
.102 MG / 5 ML
6/15/1998
ORTI-VITE CAP
seroyal international inc.
00829382
Capsule - Oral
66.67 MCG
12/31/1992

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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