Active Ingredient: MONTELUKAST SODIUM
Proprietary Name: MONTELUKAST SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A205683
Product Number: 001
Approval Date: Jan 12, 2016
Applicant Holder Full Name: ANBISON LABORATORY CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information