Active Ingredient: CARBIDOPA; LEVODOPA
Proprietary Name: CARBIDOPA AND LEVODOPA
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 50MG;200MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076663
Product Number: 001
Approval Date: Jun 24, 2004
Applicant Holder Full Name: KV PHARMACEUTICAL CO
Marketing Status:
Discontinued
Patent and Exclusivity Information