TGA Approval

PRAMOLE XR pramipexole dihydrochloride monohydrate 3 mg modified release tablet blister pack (225630)

ARTG ID

225630

ARTG Name

PRAMOLE XR pramipexole dihydrochloride monohydrate 3 mg modified release tablet blister pack

Sponsor

Arrotex Pharmaceuticals Pty Ltd

ARTG Date

June 17, 2015

Registration Type

Medicine

Therapeutic Good Type

Medicine

Licence Status

Active

Licence Category

Registered

Sponsor Information

Sponsor Name

Sponsor Item Name

Arrotex Pharmaceuticals Pty Ltd.

Ingredient Name

pramipexole dihydrochloride monohydrate

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PRAMOLE XR pramipexole dihydrochloride monohydrate 3 mg modified release tablet blister pack (225630) - TGA 批准文号 | MedPath