Active Ingredient: HYDRALAZINE HYDROCHLORIDE
Proprietary Name: HYDRALAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088517
Product Number: 001
Approval Date: Aug 22, 1985
Applicant Holder Full Name: SOLOPAK LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information