MedPath

Copper

Generic Name
Copper
Brand Names
Paragard T 380a, Vitafol-one, Cuprymina
Drug Type
Small Molecule
Chemical Formula
Cu
CAS Number
7440-50-8
Unique Ingredient Identifier
789U1901C5

Overview

Copper is a transition metal and a trace element in the body. It is important to the function of many enzymes including cytochrome c oxidase, monoamine oxidase and superoxide dismutase . Copper is commonly used in contraceptive intrauterine devices (IUD) .

Indication

For use in the supplementation of total parenteral nutrition and in contraception with intrauterine devices .

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/12/16
Phase 1
Recruiting
2024/01/31
Phase 3
Active, not recruiting
2024/01/31
Phase 3
Recruiting
2023/08/30
Phase 4
Recruiting
2023/02/15
Early Phase 1
Withdrawn
City of Hope Medical Center
2022/02/18
Early Phase 1
Recruiting
City of Hope Medical Center
2021/03/24
Phase 4
Completed
2020/02/11
Phase 2
Withdrawn
National Cancer Institute, Slovakia
2019/08/30
N/A
AVAILABLE
2018/05/31
Early Phase 1
Completed
City of Hope Medical Center

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Teva Women's Health LLC
51285-204
INTRAUTERINE
313.4 mg in 1 1
6/5/2023
METHOD PHARMACEUTICALS, LLC
58657-170
ORAL
2 mg in 1 1
12/10/2023
Everett Laboratories, Inc.
0642-0092
ORAL
2 mg in 1 1
4/18/2012
Everett Laboratories, Inc.
0642-0070
ORAL
2 mg in 1 1
9/1/2021
CooperSurgical, Inc.
59365-5128
INTRAUTERINE
313.4 mg in 1 1
1/14/2021
King Bio Inc.
57955-5122
ORAL
10 [hp_X] in 59 mL
5/19/2025
Acella Pharmaceuticals, LLC
42192-374
ORAL
2 mg in 1 1
10/11/2023
Pharmics, Inc.
0813-0202
ORAL
2 mg in 1 1
9/6/2012
Bryant Ranch Prepack
63629-3545
ORAL
2 mg in 1 1
7/17/2014
Exeltis USA, Inc.
0642-0079
ORAL
2 mg in 1 1
12/31/2022

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
No HSA approvals found for this drug.

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
DANMOT HERBALIX CHELATION FORMULA tablet bulk
52268
Danmot Pty Ltd
Medicine
A
4/18/1995

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