Active Ingredient: VANCOMYCIN HYDROCHLORIDE
Proprietary Name: VANCOMYCIN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A203300
Product Number: 002
Approval Date: Aug 11, 2020
Applicant Holder Full Name: HIKMA FARMACEUTICA PORTUGAL SA
Marketing Status:
Prescription
Patent and Exclusivity Information