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. |
Help Us Improve
Your feedback helps us provide better drug information and insights.