Overview
Antimony potassium tartrate is a schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
Indication
No indication information available.
Associated Conditions
- Cough
- Dry throat
- Phlegm
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 |
|---|---|---|---|---|---|
| Deseret Biologicals, Inc. | 43742-2108 | ORAL | 12 [hp_X] in 1 mL | 5/27/2025 | |
| Deseret Biologicals, Inc. | 43742-2218 | ORAL | 30 [hp_X] in 1 mL | 5/27/2025 | |
| Bestmade Natural Products | 82969-5010 | ORAL | 30 [hp_C] in 30 [hp_C] | 5/27/2025 | |
| King Bio Inc. | 57955-2828 | ORAL | 10 [hp_X] in 59 mL | 5/20/2025 | |
| Vsf2 Inc. | 86100-0014 | ORAL | 10 [hp_X] in 59 mL | 8/12/2025 | |
| Newton Laboratories, Inc. | 55714-1736 | ORAL | 15 [hp_X] in 1 g | 5/7/2025 | |
| Uriel Pharmacy Inc. | 48951-8084 | ORAL | 8 [hp_X] in 1 mL | 8/1/2025 | |
| Newton Laboratories, Inc. | 55714-1536 | ORAL | 15 [hp_X] in 1 mL | 5/7/2025 |
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 |
|---|---|---|---|---|---|
| APIS-HOMACCORD | 02229864 | Drops - Oral | 4 D / 100 ML | 6/1/1997 | |
| ANTIMONIUM TARTARICUM | boericke and tafel inc. | 02232099 | Globules
,
Tablet - Sublingual | 6 X | 3/1/1998 |
| HEEL 025 TAB | 01969307 | Tablet - Oral | 4 D / TAB | 12/31/1992 | |
| COU COMPLEX DPS | thompson's homeopathic supplies ltd. | 00757233 | Drops - Oral | 6 X / X | 12/31/1987 |
| ANTIMONIUM TARTARICUM GOUTTE 2CH - 30CH | boiron laboratoires | 00686646 | Drops - Oral | 2 CH / CH | 12/31/1987 |
| ANTIMONIUM TARTARICUM | homeocan inc. | 02233892 | Globules
,
Granules
,
Drops - Oral | 3 X | 1/24/1998 |
| HP12 DPS | 01975927 | Drops - Oral | 12 X / ML | 10/4/1996 | |
| HYLAND'S KINDER-CS LIQ | standard homeopathic international co | 01963252 | Liquid - Oral | 6 X / ML | 10/7/1997 |
| PNEU HP | bio active canada ltd. | 02233666 | Liquid - Oral | 30 X | 5/26/1998 |
| HP13 DPS | 01975919 | Drops - Oral | 12 X / ML | 10/4/1996 |
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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