Overview
Ammonium lactate is the ammonium salt of lactic acid.
Indication
For the treatment of dry, scaly skin (xerosis) and ichthyosis vulgaris and for temporary relief of itching associated with these conditions.
Associated Conditions
- Ichthyosis Vulgaris
- Xerosis
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2019/10/15 | Phase 3 | Completed | |||
2010/04/27 | Phase 4 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Taro Pharmaceuticals U.S.A., Inc. | 51672-1300 | TOPICAL | 120 mg in 1 g | 1/12/2024 | |
Bryant Ranch Prepack | 63629-8609 | TOPICAL | 12 g in 100 g | 7/17/2023 | |
Bryant Ranch Prepack | 63629-8611 | TOPICAL | 12 g in 100 g | 7/17/2023 | |
Padagis Israel Pharmaceuticals Ltd | 45802-493 | TOPICAL | 12 g in 100 g | 1/6/2017 | |
Taro Pharmaceuticals U.S.A., Inc. | 51672-1301 | TOPICAL | 120 mg in 1 g | 8/17/2022 | |
Bryant Ranch Prepack | 63629-8610 | TOPICAL | 12 g in 100 g | 7/17/2023 | |
Padagis Israel Pharmaceuticals Ltd | 45802-419 | TOPICAL | 12 g in 100 g | 6/7/2017 | |
Bryant Ranch Prepack | 72162-1407 | TOPICAL | 12 g in 100 g | 2/8/2024 | |
Physicians Total Care, Inc. | 54868-4599 | TOPICAL | 12 g in 100 g | 4/18/2012 | |
Bryant Ranch Prepack | 63629-8608 | TOPICAL | 12 g in 100 g | 7/17/2023 |
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 |
---|---|---|---|---|---|
EGODERM CREAM | SIN05199P | CREAM | 1% w/w | 11/16/1990 |
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 |
---|---|---|---|---|---|
No Health Canada approvals found for this drug. |
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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