Active Ingredient: VERAPAMIL HYDROCHLORIDE
Proprietary Name: VERAPAMIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 120MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071489
Product Number: 001
Approval Date: Jan 13, 1988
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information