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: A077809
Product Number: 002
Approval Date: Nov 30, 2010
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Proprietary Name: CIPROFLOXACIN EXTENDED RELEASE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 425.2MG;EQ 574.9MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077809
Product Number: 001
Approval Date: Nov 30, 2010
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information