Active Ingredient: LINEZOLID
Proprietary Name: LINEZOLID
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078987
Product Number: 001
Approval Date: Dec 21, 2015
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS SA
Marketing Status:
Prescription
Patent and Exclusivity Information