Active Ingredient: CLONIDINE HYDROCHLORIDE
Proprietary Name: CLONIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 0.1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A210052
Product Number: 001
Approval Date: Nov 20, 2017
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS OF NY LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information