Active Ingredient: CLONIDINE HYDROCHLORIDE
Proprietary Name: CLONIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071103
Product Number: 001
Approval Date: Aug 14, 1986
Applicant Holder Full Name: DURAMED PHARMACEUTICALS INC SUB BARR LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information