Overview
No overview information available.
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 |
|---|---|---|---|---|---|
| Teva Pharmaceuticals USA, Inc. | 0093-3123 | ORAL | 250 mg in 1 1 | 6/22/2022 | |
| Aurobindo Pharma Limited | 59651-566 | ORAL | 500 mg in 1 1 | 12/27/2023 | |
| Liberty Pharmaceuticals, Inc. | 0440-1380 | ORAL | 250 mg in 1 1 | 9/23/2013 | |
| Asclemed USA, Inc. | 76420-183 | ORAL | 500 mg in 1 1 | 11/14/2020 | |
| RedPharm Drug, Inc. | 67296-1205 | ORAL | 500 mg in 1 1 | 1/20/2022 | |
| A-S Medication Solutions | 50090-0116 | ORAL | 250 mg in 1 1 | 6/22/2022 | |
| H.J. Harkins Company, Inc. | 52959-049 | ORAL | 500 mg in 1 1 | 12/7/2011 | |
| Aidarex Pharmaceuticals LLC | 33261-167 | ORAL | 250 mg in 1 1 | 6/23/2016 | |
| NuCare Pharmaceticals, Inc. | 66267-073 | ORAL | 500 mg in 1 1 | 1/13/2022 | |
| Aurobindo Pharma Limited | 59651-565 | ORAL | 250 mg in 1 1 | 12/27/2023 |
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 |
|---|---|---|---|---|---|
| DISTAPH 500 dicloxacillin 500mg (as sodium) capsule bottle | 226508 | Medicine | A | 10/28/2014 | |
| DICLOSTAPH dicloxacillin (as sodium) 500 mg capsule bottle | 410935 | Medicine | A | 7/21/2023 | |
| DICLOXACILLIN VIATRIS 250 dicloxacillin (as sodium) 250 mg capsule bottle | 289105 | Medicine | A | 7/20/2017 | |
| APX-DICLOXACILLIN dicloxacillin (as sodium) 500 mg capsule bottle | 391295 | Medicine | A | 7/21/2023 | |
| ARX-DICLOXACILLIN dicloxacillin (as sodium) 500 mg capsule bottle | 391292 | Medicine | A | 7/21/2023 | |
| ARX-DICLOXACILLIN dicloxacillin (as sodium) 250 mg capsule bottle | 391293 | Medicine | A | 7/21/2023 | |
| DICLOXSIG dicloxacillin (as sodium) 500mg capsule bottle | 162745 | Medicine | A | 9/7/2009 | |
| DICLOXIAN dicloxacillin (as sodium) 500 mg capsule bottle | 391291 | Medicine | A | 7/21/2023 | |
| KLOXALIN dicloxacillin (as sodium) 250 mg capsule bottle | 391297 | Medicine | A | 7/21/2023 | |
| APX-DICLOXACILLIN dicloxacillin (as sodium) 250 mg capsule bottle | 391294 | Medicine | A | 7/21/2023 |
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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