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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: A078605
Product Number: 001
Approval Date: Aug 3, 2012
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information