Active Ingredient: CIPROFLOXACIN HYDROCHLORIDE
Proprietary Name: CIPROFLOXACIN HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OTIC
Strength: EQ 0.2% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A217887
Product Number: 001
Approval Date: Nov 5, 2024
Applicant Holder Full Name: IDENTIRX LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
