Active Ingredient: MOEXIPRIL HYDROCHLORIDE
Proprietary Name: MOEXIPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 7.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090416
Product Number: 001
Approval Date: Mar 30, 2010
Applicant Holder Full Name: GLENMARK PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information