Active Ingredient: CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Proprietary Name: CIPROFLOXACIN EXTENDED RELEASE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 212.6MG;EQ 287.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A078712
Product Number: 001
Approval Date: Dec 11, 2007
Applicant Holder Full Name: FOSUN PHARMA USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
