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Active Ingredient: VORICONAZOLE
Proprietary Name: VORICONAZOLE
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: 200MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A211264
Product Number: 001
Approval Date: Mar 9, 2023
Applicant Holder Full Name: UBI PHARMA INC
Marketing Status:
Prescription
Patent and Exclusivity Information