Active Ingredient: FLUORESCEIN SODIUM
Proprietary Name: FLUORESCEIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: EQ 500MG BASE/2ML (EQ 250MG BASE/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A215709
Product Number: 002
Approval Date: Sep 25, 2023
Applicant Holder Full Name: NEXUS PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
