Active Ingredient: CARBIDOPA; LEVODOPA
Proprietary Name: CARBIDOPA AND LEVODOPA
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 25MG;100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A076212
Product Number: 001
Approval Date: Jun 16, 2004
Applicant Holder Full Name: APOTEX INC
Marketing Status:
Prescription
Patent and Exclusivity Information