Active Ingredient: HYDRALAZINE HYDROCHLORIDE
Proprietary Name: HYDRALAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088671
Product Number: 001
Approval Date: May 1, 1984
Applicant Holder Full Name: QUANTUM PHARMICS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information