Product Details for ANDA 075389
AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
100MG
Marketing Status: Prescription
200MG
Marketing Status: Prescription
400MG
Marketing Status: Prescription
100MG
Marketing Status: Prescription
Active Ingredient: AMIODARONE HYDROCHLORIDE
Proprietary Name: AMIODARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075389
Product Number: 002
Approval Date: Dec 28, 2017
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status: Prescription
Patent and Exclusivity Information
AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
Proprietary Name: AMIODARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075389
Product Number: 002
Approval Date: Dec 28, 2017
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status: Prescription
Patent and Exclusivity Information
200MG
Marketing Status: Prescription
Active Ingredient: AMIODARONE HYDROCHLORIDE
Proprietary Name: AMIODARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075389
Product Number: 001
Approval Date: Jan 25, 2001
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status: Prescription
Patent and Exclusivity Information
AMIODARONE HYDROCHLORIDE (AMIODARONE HYDROCHLORIDE)
Proprietary Name: AMIODARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075389
Product Number: 001
Approval Date: Jan 25, 2001
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status: Prescription
Patent and Exclusivity Information
400MG
Marketing Status: Prescription
Active Ingredient: AMIODARONE HYDROCHLORIDE
Proprietary Name: AMIODARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075389
Product Number: 003
Approval Date: Dec 28, 2017
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: AMIODARONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 400MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075389
Product Number: 003
Approval Date: Dec 28, 2017
Applicant Holder Full Name: DR REDDYS LABORATORIES SA
Marketing Status: Prescription
Patent and Exclusivity Information