Active Ingredient: LEVOCETIRIZINE DIHYDROCHLORIDE
Proprietary Name: LEVOCETIRIZINE DIHYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A211551
Product Number: 001
Approval Date: Nov 20, 2018
Applicant Holder Full Name: MICRO LABS LTD
Marketing Status:
Over-the-counter
Patent and Exclusivity Information