Active Ingredient: HYDRALAZINE HYDROCHLORIDE
Proprietary Name: HYDRALAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088177
Product Number: 001
Approval Date: Jul 29, 1983
Applicant Holder Full Name: PUREPAC PHARMACEUTICAL CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
