Visitor Monitoring Drug Details: REQUIP
 
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Drug Details

Drug Name: REQUIP
FDA Application No: (NDA) 020658
Active Ingredient(s): ROPINIROLE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: September 19, 1997
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
REQUIP ROPINIROLE HYDROCHLORIDEEQ 0.25MG BASETABLET; ORAL Prescription Yes None
REQUIP ROPINIROLE HYDROCHLORIDEEQ 0.5MG BASETABLET; ORAL Prescription No None
REQUIP ROPINIROLE HYDROCHLORIDEEQ 1MG BASETABLET; ORAL Prescription No None
REQUIP ROPINIROLE HYDROCHLORIDEEQ 2MG BASETABLET; ORAL Prescription No None
REQUIP ROPINIROLE HYDROCHLORIDEEQ 5MG BASETABLET; ORAL Prescription No None
REQUIP ROPINIROLE HYDROCHLORIDEEQ 3MG BASETABLET; ORAL Prescription No None
REQUIP ROPINIROLE HYDROCHLORIDEEQ 4MG BASETABLET; ORAL Prescription No None


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