Active Ingredient: MIDAZOLAM HYDROCHLORIDE
Proprietary Name: MIDAZOLAM HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A075247
Product Number: 002
Approval Date: Jun 23, 2000
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
