Active Ingredient: ALPRAZOLAM
Proprietary Name: ALPRAZOLAM
Dosage Form; Route of Administration: CONCENTRATE; ORAL
Strength: 1MG/ML
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A074312
Product Number: 001
Approval Date: Oct 31, 1993
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information