BACTROBAN

This brand name is authorized in Austria, Australia, Brazil, Cyprus, Estonia, Spain, Finland, France, Hong Kong, Ireland, Israel, Japan, Malta, Mexico, New Zealand, Poland, Singapore, Tunisia, Turkey, United Kingdom, South Africa

Active ingredients

The drug BACTROBAN contains one active pharmaceutical ingredient (API):

1 Mupirocin
UNII RG38I2P540 - MUPIROCIN CALCIUM

Mupirocin is a novel antibiotic produced through fermentation by Pseudomonas fluorescens. Mupirocin inhibits isoleucyl transfer-RNA synthetase, thereby arresting bacterial protein synthesis. Mupirocin has bacteriostatic properties at minimum inhibitory concentrations and bactericidal properties at the higher concentrations reached when applied locally.

Read about Mupirocin

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BACTROBAN 2% Cream Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC
BACTROBAN Nasal ointment Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
D06AX09 Mupirocin D Dermatologicals → D06 Antibiotics and chemotherapeutics for dermatological use → D06A Antibiotics for topical use → D06AX Other antibiotics for topical use
Discover more medicines within D06AX09
R01AX06 Mupirocin R Respiratory system → R01 Nasal preparations → R01A Decongestants and other nasal preparations for topical use → R01AX Other nasal preparations
Discover more medicines within R01AX06

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 4348W, 4350Y, 9440W
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 510601301160316, 510614020051403
Country: EE Ravimiamet Identifier(s): 1110283, 1272743, 1865224
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 58868, 59531
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 545681, 568709
Country: FR Base de données publique des médicaments Identifier(s): 66325311
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 138358, 142019, 142021, 161401, 165417, 165419, 29069, 29081, 29085
Country: HK Department of Health Drug Office Identifier(s): 28186, 33588
Country: IE Health Products Regulatory Authority Identifier(s): 13716, 13765, 13773, 36830
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 976, 977
Country: JP 医薬品医療機器総合機構 Identifier(s): 6119700M1035
Country: MT Medicines Authority Identifier(s): MA192/02401, MA192/02402, MA192/02403, PI908/10601A
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 037M86
Country: NL Z-Index G-Standaard Identifier(s): 13250728, 13577395
Country: NL Z-Index G-Standaard, PRK Identifier(s): 21156, 32085
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 4227
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100008702, 100008719, 100098125, 100162952, 100241723, 100241746, 100272221, 100298717, 100298976, 100304398, 100324484, 100366146, 100384865, 100384888, 100394177, 100396816, 100399051, 100405053, 100421595, 100425185, 100427563, 100431820, 100437202, 100443740, 100459033, 100460327
Country: SG Health Sciences Authority Identifier(s): 00554P, 05075P, 11204P
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 5143011
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699522355426, 8699522358014, 8699522385522, 8699522385539
Country: ZA Health Products Regulatory Authority Identifier(s): 34/20.1.6/0274, T/20.1.6/0075, W/20.1.6/218

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