RIFADIN

This brand name is authorized in United States. It is also authorized in Australia, Estonia, Hong Kong SAR China, Ireland, Japan, Malta, Mexico, Netherlands, New Zealand, South Africa, UK.

Active ingredients

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

1
UNII VJT6J7R4TR - RIFAMPIN
 

Rifampicin is an active bactericidial antituberculosis drug which is particularly active against the rapidly growing extracellular organisms and also has bactericidial activity intracellularly. Rifampicin inhibits DNA-dependent RNA polymerase activity in susceptible cells. Specifically, it interacts with bacterial RNA polymerase but does not inhibit the mammalian enzyme.

 
Read more about Rifampicin

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 RIFADIN Capsule MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)
 RIFADIN Solvent MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
J04AB02 Rifampicin J Antiinfectives for systemic use → J04 Antimycobacterials → J04A Drugs for treatment of tuberculosis → J04AB Antibiotics
Discover more medicines within J04AB02
J04AB03 Rifamycin J Antiinfectives for systemic use → J04 Antimycobacterials → J04A Drugs for treatment of tuberculosis → J04AB Antibiotics
Discover more medicines within J04AB03

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 8025J
EE Ravimiamet 1638626, 1742712, 1858776
GB Medicines & Healthcare Products Regulatory Agency 19103, 19129, 19135, 44017
HK Department of Health Drug Office 28161, 28162, 28163
IE Health Products Regulatory Authority 43990, 44008, 84077
JP 医薬品医療機器総合機構 6164001M1216
MT Medicines Authority AA565/04102, AA565/04103, AA565/04104, AA565/04105, MA1359/02701, PI565/04107A
MX Comisión Federal para la Protección contra Riesgos Sanitarios 69441, 70964
NL Z-Index G-Standaard 14044269, 14044285
NL Z-Index G-Standaard, PRK 21237, 264, 7064, 7072
NZ Medicines and Medical Devices Safety Authority 1175, 1178, 1179, 1180
US FDA, National Drug Code 0068-0508, 0068-0510, 0068-0597, 0068-0599
ZA Health Products Regulatory Authority B/20.1.1/2, B/20.1.1/3

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