Overview
A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis. Except for radioactive forms of cobalt and cobalamin, the FDA withdrew its approval for the use of drug products containing cobalt salts.
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 |
|---|---|---|---|---|---|
| King Bio Inc. | 57955-2822 | ORAL | 10 [hp_X] in 59 mL | 5/20/2025 | |
| Deseret Biologicals, Inc. | 43742-1312 | ORAL | 8 [hp_X] in 1 mL | 5/27/2025 | |
| Dr. Donna Restivo DC | 62185-0062 | ORAL | 8 [hp_X] in 1 mL | 5/23/2025 | |
| Dr. Donna Restivo DC | 62185-0065 | ORAL | 12 [hp_X] in 1 mL | 5/23/2025 |
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 |
|---|---|---|---|---|---|
| APIZELEN | bio active canada ltd. | 02233553 | Liquid - Oral | 12 X | 5/26/1998 |
| CATALIGO FER-CUIVRE-COBALT - LIQ | laboratoires holis inc. | 02132265 | Liquid - Oral | 6 X / ML | 12/31/1986 |
| DIATHESIS V-2 | bio active canada ltd. | 02234230 | Liquid - Oral | 8 X | 5/26/1998 |
| N.S.K.I. | n.e.o.m. | 02063832 | Tablet - Oral | 4 C / TAB | 10/18/1996 |
| COBALTUM METALLICUM DROPS 5CH-30CH | dolisos laboratoires s.a. | 00745065 | Drops - Oral | 4 CH / CH | 12/31/1987 |
| COBALTUM METALLICUM | dolisos canada inc. | 02234424 | Granules
,
Globules
,
Liquid - Oral | 6 X | 1/5/1998 |
| CATALIGO ZINC-NICKEL-COBALT-LIQ | laboratoires holis inc. | 02132249 | Liquid - Oral | 6 X / ML | 12/31/1986 |
| CATALIGO MANGANESE-COBALT LIQ | laboratoires holis inc. | 02132257 | Liquid - Oral | 6 X / ML | 12/31/1986 |
| COBALTUM METALLICUM | total health centre | 02236276 | Drops - Oral | 6 X | 1/4/1998 |
| COBALTUM METALLICUM-INJEEL LIQ (12D,30D,200D/1.1ML) | 02057980 | Liquid - Oral | 12 D / 1.1 ML | 12/31/1993 |
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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