Active Ingredient: METHYLDOPA
Proprietary Name: METHYLDOPA
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018934
Product Number: 001
Approval Date: Jun 29, 1984
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information