Active Ingredient: DILTIAZEM HYDROCHLORIDE
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A202651
Product Number: 001
Approval Date: Aug 9, 2012
Applicant Holder Full Name: HIKMA FARMACEUTICA PORTUGAL SA
Marketing Status:
Discontinued
Patent and Exclusivity Information
