|
|
H2014/CTD1132/030
|
PRAMIPEX 1
|
PRAMIPEXOLE DIHYDROCHLORIDE
|
SUN PHARMA EAST AFRICA LTD
|
Registered
|
Details →
|
|
|
H2014/CTD1967/438
|
PRAMIPEX 0.5
|
PRAMIPEXOLE DIHYDROCHLORIDE
|
SUN PHARMA EAST AFRICA LTD
|
Registered
|
Details →
|
|
|
H2014/CTD1133/038
|
PRAMIPEX 0.25
|
PRAMIPEXOLE DIHYDROCHLORIDE
|
SUN PHARMA EAST AFRICA LTD
|
Registered
|
Details →
|
|
|
H2014/CTD482/130
|
RAMIPEX 1MG TABLET
|
PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
|
MEDOX PHARMACEUTICALS LIMITED
|
Registered
|
Details →
|
|
|
H2008/19570/548
|
PEXOLA 1,0 MG TABLETS
|
PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
|
Withdrawn Voluntarily by Market Authorization Holder for Commercial reasons only. Withdrawal is not due to quality and safety issues.
|
|
Details →
|
|
|
H2008/19569/547
|
PEXOLA 0,25 MG TABLETS
|
PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
|
Withdrawn Voluntarily by Market Authorization Holder for Commercial reasons only. Withdrawal is not due to quality and safety issues.
|
|
Details →
|
|
|
H2015/CTD/479/584
|
RAMIPEX 0.25MG TABLETS
|
PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
|
MEDOX PHARMACEUTICALS LIMITED
|
Registered
|
Details →
|
|
|
H2008/19521/503
|
PEXOLA 0,125 MG TABLETS
|
PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
|
Withdrawn Voluntarily by Market Authorization Holder for Commercial reasons only. Withdrawal is not due to quality and safety issues.
|
|
Details →
|