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:
Application Number: A090579
Product Number: 001
Approval Date: Jan 8, 2016
Applicant Holder Full Name: ASTRAL STERITECH PVT LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information