Active Ingredient: AZATHIOPRINE SODIUM
Proprietary Name: AZATHIOPRINE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 100MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A074419
Product Number: 001
Approval Date: Mar 31, 1995
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
