Active Ingredient: LINEZOLID
Proprietary Name: LINEZOLID
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 200MG/100ML (2MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A207354
Product Number: 001
Approval Date: Dec 20, 2016
Applicant Holder Full Name: NANG KUANG PHARMACEUTICAL CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information