Active Ingredient: HYDROXYZINE HYDROCHLORIDE
Proprietary Name: HYDROXYZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088529
Product Number: 001
Approval Date: Oct 22, 1985
Applicant Holder Full Name: QUANTUM PHARMICS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
