Active Ingredient: CARBIDOPA; LEVODOPA
Proprietary Name: CARBIDOPA AND LEVODOPA
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A073589
Product Number: 001
Approval Date: Aug 28, 1992
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status:
Prescription
Patent and Exclusivity Information
