Active Ingredient: HYDROXYZINE HYDROCHLORIDE
Proprietary Name: HYDROXYZINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A087593
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SOLOPAK LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
