Active Ingredient: LEVOCETIRIZINE DIHYDROCHLORIDE
Proprietary Name: LEVOCETIRIZINE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 2.5MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A210914
Product Number: 001
Approval Date: Apr 1, 2019
Applicant Holder Full Name: HETERO LABS LTD UNIT III
Marketing Status:
Prescription
Patent and Exclusivity Information
