Active Ingredient: METRONIDAZOLE
Proprietary Name: METRONIDAZOLE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 500MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A206191
Product Number: 001
Approval Date: Feb 25, 2019
Applicant Holder Full Name: INFORLIFE SA
Marketing Status:
Prescription
Patent and Exclusivity Information
