Active Ingredient: MEROPENEM
Proprietary Name: MEROPENEM AND SODIUM CHLORIDE IN DUPLEX CONTAINER
Dosage Form; Route of Administration: POWDER; INTRAVENOUS
Strength: 500MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N202106
Product Number: 001
Approval Date: Apr 30, 2015
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information