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NDC 43547-0272-10

ropinirole hydrochloride 3 mg/1 TABLET, FILM COATED

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NDC
43547-0272-10
Generic Name
ropinirole hydrochloride
Brand Name
ropinirole hydrochloride
Strength
3 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
Labeler
SOLCO HEALTHCARE US, LLC

FDA Drug Information

Indications & Usage

1 INDICATIONS AND USAGE Ropinirole tablets are a non-ergoline dopamine agonist indicated for the treatment of Parkinson’s disease (PD) and moderate-to-severe primary Restless Legs Syndrome (RLS). ( 1.1 , 1.2 ) 1.1 Parkinson’s Disease Ropinirole tablets are indicated for the treatment of Parkinson's disease. 1.2 Restless Legs Syndrome Ropinirole tablets are indicated for the treatment of moderate-to-severe primary Restless Legs Syndrome (RLS).

Source: FDA. For professional use only. Not a substitute for prescribing information.

Other ropinirole hydrochloride NDC Codes

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