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: AB
Application Number: A090199
Product Number: 001
Approval Date: Aug 22, 2011
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information