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: A074894
Product Number: 001
Approval Date: Aug 26, 1997
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information