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: A072138
Product Number: 001
Approval Date: Jun 13, 1988
Applicant Holder Full Name: WARNER CHILCOTT DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information