Active Ingredient: NICARDIPINE HYDROCHLORIDE
Proprietary Name: NICARDIPINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 25MG/10ML (2.5MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N078405
Product Number: 001
Approval Date: Nov 17, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
