Active Ingredient: ALPROSTADIL
Proprietary Name: ALPROSTADIL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.5MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A074815
Product Number: 001
Approval Date: Jan 20, 1998
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
