Active Ingredient: DILTIAZEM HYDROCHLORIDE
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 360MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A209766
Product Number: 001
Approval Date: May 30, 2018
Applicant Holder Full Name: PAR PHARMACEUTICAL
Marketing Status:
Discontinued
Patent and Exclusivity Information