MedPath

Cloxacillin

Generic Name
Cloxacillin
Drug Type
Small Molecule
Chemical Formula
C19H18ClN3O5S
CAS Number
61-72-3
Unique Ingredient Identifier
O6X5QGC2VB

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

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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