MedPath

Molybdenum

Generic Name
Molybdenum
Drug Type
Small Molecule
Chemical Formula
Mo
CAS Number
7439-98-7
Unique Ingredient Identifier
81AH48963U

Overview

Molybdenum is a chemical element with symbol Mo and atomic number 42. As it is not a naturally occuring free metal on Earth, molybdenum is found only in various oxidation states in minerals. Molybdenum is commonly used in metallurgy and other chemical applications however it has essential biological roles in organisms and microorganisms. It is an essential trace dietary element and acts as a critical cofactor in several molybdenum-dependent enzymes that are involved in important cellular reactions and pathways, including xanthine oxidoreductase. When complexed with Technetium Tc 99m, molybdenum is used as a radiopharmaceutical agent in diagonistic procedures.

Indication

No indication information available.

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
PureTek Corporation
59088-193
ORAL
45 ug in 1 1
1/11/2023
Novian Pharmaceuticals
83146-003
ORAL
45 ug in 1 1
10/6/2023
PureTek Corporation
59088-166
ORAL
50 ug in 1 1
2/8/2023
PureTek Corporation
59088-180
ORAL
25 ug in 1 1
1/11/2023
PureTek Corporation
59088-187
ORAL
45 ug in 1 1
1/11/2023
PureTek Corporation
59088-525
ORAL
45 ug in 1 1
2/16/2022
PureTek Corporation
59088-181
ORAL
25 ug in 1 1
1/11/2023
PureTek Corporation
59088-165
ORAL
45 ug in 1 1
1/11/2023
PureTek Corporation
59088-480
ORAL
25 ug in 1 1
1/11/2023
PureTek Corporation
59088-168
ORAL
45 ug in 1 1
1/11/2023

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
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
ONE A DAY ADVANCE ADULTS 50 PLUS TAB
miles canada inc. - consumer health care division
02080702
Tablet - Oral
10 MCG / TAB
12/31/1994
MOLYBDENUM METALLICUM GRANULES 4CH-30CH
dolisos laboratoires s.a.
00769711
Tablet - Oral
4 CH / CH
12/31/1988
ONE A DAY ADVANCE ADULTS TAB
miles canada inc. - consumer health care division
02080710
Tablet - Oral
10 MCG / TAB
12/31/1994

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
HIDROPOLIVIT A MINERAL COMPRIMIDOS MASTICABLES
Laboratorios Menarini S.A.
44019
COMPRIMIDO MASTICABLE
Sin Receta
Not Commercialized

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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