Overview
Tartaric acid is a white crystalline organic acid that occurs naturally in many plants, most notably in grapes.Tartaric is an alpha-hydroxy-carboxylic acid, is diprotic and aldaric in acid characteristics, and is a dihydroxyl derivative of succinic acid.
Indication
Tartaric Acid is primarily indicated in conditions like Antiscorbutic, Antiseptic.
Associated Conditions
- Dyspepsia
- Dysuria
- Heartburn
- Kidney Stones
- Pain
- Upset stomach
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 |
---|---|---|---|---|---|
No FDA approvals found for this drug. |
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 |
---|---|---|---|---|---|
Ural Effervescent Granules | SIN14374P | GRANULE, EFFERVESCENT | 0.89g | 6/26/2013 |
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 |
---|---|---|---|---|---|
BAROS EFFERVESCENT GRANULES | N/A | N/A | N/A | 9/6/1988 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
APOHEALTH Cystitis Relief oral powder sachet | 227717 | Medicine | A | 9/8/2014 | |
Chemists' Own Cystitis Relief effervescent granules sachet | 297741 | Medicine | A | 12/19/2017 | |
URIZ URINARY ALKALINISER effervescent granules oral powder sachet | 314267 | Medicine | A | 2/15/2019 | |
PHARMACY HEALTH CYSTITIS RELIEF powder for oral liquid sachet | 314974 | Medicine | A | 3/1/2019 | |
URACT CRANBERRY FLAVOUR EFFERVESCENT POWDER oral sachet | 482087 | Medicine | A | 3/7/2025 | |
AMCAL URICALM EFFERVESCENT CYSTITIS RELIEF powder for oral liquid sachet | 479007 | Medicine | A | 2/14/2025 | |
GUARDIAN URICALM EFFERVESCENT CYSTITIS RELIEF powder for oral liquid sachet | 479008 | Medicine | A | 2/14/2025 | |
AMCAL URICALM EFFERVESCENT granules oral powder sachet | 210402 | Medicine | A | 5/31/2013 | |
URAL cranberry flavour effervescent powder sachets | 308403 | Medicine | A | 8/21/2018 | |
APOHEALTH CYSTITIS RELIEF lemon flavour effervescent granules sachet | 299122 | Medicine | A | 1/30/2018 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
BAROS EFFERVESCENT GRANULES | tyco healthcare | 00776580 | Powder (Effervescent) - Oral | 420 MG / G | 12/31/1988 |
URASAL GRANULES | axxess pharma inc. | 00116866 | Powder (Effervescent) - Oral | 3.8 G / 2 TSP | 12/31/1951 |
UNIK ZORU PWR | therapex division de e-z-em canada inc | 00514594 | Powder - Oral | 1.05 G / 3 G | 12/31/1981 |
UNIK ZORU TAB | therapex division de e-z-em canada inc | 00514586 | Tablet - Oral | 52.5 MG | 12/31/1981 |
TARTARICUM ACIDUM GRANULE(1CH-30CH) | homeocan inc. | 01949861 | Tablet - Oral | 1 CH / TAB | 12/31/1991 |
E-Z-GAS 2 GRANULES | therapex division de e-z-em canada inc | 01990047 | Powder - Oral | 1.648 G / 4 G | 12/31/1985 |
TARTARICUM ACIDUM | homeocan inc. | 02234157 | Granules
,
Drops
,
Globules - Oral | 1 X | 1/22/1998 |
ACIDUM TARTARICUM-INJEEL FORTE LIQ (D6-D200) | 02036908 | Liquid - Oral | 6 D / ML | 12/31/1993 | |
ACIDUM TARTARICUM-INJEEL LIQ (D12-D200) | 02036916 | Liquid - Oral | 12 D / ML | 12/31/1993 | |
SEPTILINE | produits francais labs inc. | 00306215 | Powder (Effervescent) - Oral | 392 MG / G | 12/31/1979 |
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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