Active Ingredient: AMPICILLIN SODIUM; SULBACTAM SODIUM
Proprietary Name: AMPICILLIN AND SULBACTAM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1GM BASE/VIAL;EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A201406
Product Number: 001
Approval Date: Dec 7, 2015
Applicant Holder Full Name: ANTIBIOTICE SA
Marketing Status:
Prescription
Patent and Exclusivity Information