Active Ingredient: DIAZOXIDE
Proprietary Name: DIAZOXIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 15MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071519
Product Number: 001
Approval Date: Aug 26, 1987
Applicant Holder Full Name: ABRAXIS PHARMACEUTICAL PRODUCTS
Marketing Status:
Discontinued
Patent and Exclusivity Information
