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: A210702
Product Number: 001
Approval Date: Apr 25, 2019
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
