Active Ingredient: BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM
Proprietary Name: ALTAFLUOR BENOX
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.4%;0.25%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N208582
Product Number: 001
Approval Date: Dec 14, 2017
Applicant Holder Full Name: ALTAIRE PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
