Active Ingredient: METHYLDOPA
Proprietary Name: METHYLDOPA
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071067
Product Number: 001
Approval Date: Dec 5, 1986
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information