Active Ingredient: AMPICILLIN SODIUM; SULBACTAM SODIUM
Proprietary Name: AMPICILLIN AND SULBACTAM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A065188
Product Number: 001
Approval Date: Nov 25, 2005
Applicant Holder Full Name: HQ SPECIALTY PHARMA CORP
Marketing Status:
Prescription
Patent and Exclusivity Information
