Overview
A semi-synthetic penicillin antibiotic which is a chlorinated derivative of oxacillin.
Indication
Cloxacillin is indicated for the treatment of beta-hemolytic streptococcal, pneumococcal, and staphylococcal infections (including beta-lactamase producing organisms).
Associated Conditions
- Infection caused by staphylococci
- Infections caused by penicillinase-producing staphylococci
- Pneumococcal Infection
- Streptococcal Infections
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/12/10 | Phase 4 | Recruiting | |||
2017/08/14 | Not Applicable | Active, not recruiting | |||
2013/06/11 | Phase 3 | Terminated | Fundación Pública Andaluza Progreso y Salud | ||
2013/02/15 | Phase 3 | Completed | Heinrich-Heine University, Duesseldorf | ||
2009/04/21 | Not Applicable | Completed | |||
2005/08/12 | Not Applicable | Completed | |||
2003/06/12 | Phase 2 | Completed | Cumberland Pharmaceuticals |
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 |
---|---|---|---|---|---|
CLOXACAP 250 CAPSULE 250 mg | SIN05036P | CAPSULE | 250 mg | 8/30/1990 | |
OXACIL GRANULES 125MG/5ML | SIN09934P | GRANULE, FOR SUSPENSION | 125 mg/5 ml | 8/5/1998 | |
CLOXACILLIN PANPHARMA FOR INJECTION 500 mg/vial | SIN07168P | INJECTION, POWDER, FOR SOLUTION | 500 mg/vial | 10/8/1992 | |
MEIXAM POWDER FOR SOLUTION FOR INJECTION 500MG/VIAL | SIN15834P | INJECTION, POWDER, FOR SOLUTION | 500mg/vial | 10/21/2019 | |
CLOXACAP 500 CAPSULE 500 mg | SIN08889P | CAPSULE | 500 mg | 9/4/1996 | |
CLOXACILLIN STRAGEN POWDER FOR SOLUTION FOR INJECTION 500 MG/VIAL | SIN15001P | INJECTION, POWDER, FOR SOLUTION | 500mg | 5/3/2016 |
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 |
---|---|---|---|---|---|
ORBENIN INJ 250MG | ayerst laboratories | 00002151 | Powder For Solution - Intravenous
,
Intramuscular | 250 MG / VIAL | 12/31/1964 |
CLOXACILLIN SODIUM FOR INJECTION | teva canada limited | 01912429 | Powder For Solution - Intramuscular
,
Intravenous | 500 MG / VIAL | 12/31/1992 |
APO CLOXI CAP 250MG | 00618292 | Capsule - Oral | 250 MG | 12/31/1984 | |
ORBENIN CAP 500MG | ayerst laboratories | 00002054 | Capsule - Oral | 500 MG / CAP | 12/31/1963 |
TEGOPEN INJ 250MG/VIAL | bristol labs division of bristol-myers squibb | 00407593 | Powder For Solution - Intramuscular
,
Intravenous | 250 MG / VIAL | 12/31/1973 |
CLOXACILLIN SODIUM FOR INJECTION | teva canada limited | 01975447 | Powder For Solution - Intravenous | 1 G / VIAL | 12/31/1992 |
ORBENIN INJ 2000MG | ayerst laboratories | 00002186 | Powder For Solution - Intravenous
,
Intramuscular | 2 G / VIAL | 12/31/1966 |
ORBENIN PWR 125MG/5ML | ayerst laboratories | 00002445 | Powder For Solution - Oral | 125 MG / 5 ML | 12/31/1966 |
APO CLOXI CAP 500MG | 00618284 | Capsule - Oral | 500 MG | 12/31/1984 | |
ORBENIN CAP 250MG | ayerst laboratories | 00002046 | Capsule - Oral | 250 MG / CAP | 12/31/1963 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
CLOXACILINA IPS 1g POLVO PARA SOLUCION INYECTABLE EFG | I P S Farma S.L. | 63244 | POLVO PARA SOLUCIÓN INYECTABLE | Medicamento Sujeto A Prescripción Médica | Not Commercialized |
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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