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Active Ingredient: DIAZOXIDE
Proprietary Name: DIAZOXIDE
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 50MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211050
Product Number: 001
Approval Date: Dec 20, 2019
Applicant Holder Full Name: E5 PHARMA INC
Marketing Status:
Prescription
Patent and Exclusivity Information