Active Ingredient: AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Proprietary Name: AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 5MG BASE;40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090149
Product Number: 001
Approval Date: Jul 5, 2011
Applicant Holder Full Name: DR REDDYS LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Proprietary Name: AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 10MG BASE;40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090149
Product Number: 002
Approval Date: Jul 5, 2011
Applicant Holder Full Name: DR REDDYS LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information