Active Ingredient: HYDRALAZINE HYDROCHLORIDE
Proprietary Name: HYDRALAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088649
Product Number: 001
Approval Date: Oct 18, 1984
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
