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: A090349
Product Number: 001
Approval Date: Sep 20, 2010
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: AMPICILLIN SODIUM; SULBACTAM SODIUM
Proprietary Name: AMPICILLIN AND SULBACTAM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A090349
Product Number: 002
Approval Date: Sep 20, 2010
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information