Active Ingredient: NICARDIPINE HYDROCHLORIDE
Proprietary Name: NICARDIPINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074540
Product Number: 001
Approval Date: Oct 28, 1996
Applicant Holder Full Name: ANI PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information