Active Ingredient: CARBIDOPA; ENTACAPONE; LEVODOPA
Proprietary Name: CARBIDOPA, LEVODOPA AND ENTACAPONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;200MG;100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A079085
Product Number: 001
Approval Date: May 10, 2012
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: CARBIDOPA; ENTACAPONE; LEVODOPA
Proprietary Name: CARBIDOPA, LEVODOPA AND ENTACAPONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 37.5MG;200MG;150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A079085
Product Number: 002
Approval Date: May 10, 2012
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information