Product Details for ANDA 211049
OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL)
5MG
Marketing Status: Prescription
20MG
Marketing Status: Prescription
40MG
Marketing Status: Prescription
5MG
Marketing Status: Prescription
Active Ingredient: OLMESARTAN MEDOXOMIL
Proprietary Name: OLMESARTAN MEDOXOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211049
Product Number: 001
Approval Date: Feb 22, 2019
Applicant Holder Full Name: SUNSHINE LAKE PHARMA CO LTD
Marketing Status: Prescription
Patent and Exclusivity Information
OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL)
Proprietary Name: OLMESARTAN MEDOXOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211049
Product Number: 001
Approval Date: Feb 22, 2019
Applicant Holder Full Name: SUNSHINE LAKE PHARMA CO LTD
Marketing Status: Prescription
Patent and Exclusivity Information
20MG
Marketing Status: Prescription
Active Ingredient: OLMESARTAN MEDOXOMIL
Proprietary Name: OLMESARTAN MEDOXOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211049
Product Number: 002
Approval Date: Feb 22, 2019
Applicant Holder Full Name: SUNSHINE LAKE PHARMA CO LTD
Marketing Status: Prescription
Patent and Exclusivity Information
OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL)
Proprietary Name: OLMESARTAN MEDOXOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211049
Product Number: 002
Approval Date: Feb 22, 2019
Applicant Holder Full Name: SUNSHINE LAKE PHARMA CO LTD
Marketing Status: Prescription
Patent and Exclusivity Information
40MG
Marketing Status: Prescription
Active Ingredient: OLMESARTAN MEDOXOMIL
Proprietary Name: OLMESARTAN MEDOXOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211049
Product Number: 003
Approval Date: Feb 22, 2019
Applicant Holder Full Name: SUNSHINE LAKE PHARMA CO LTD
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: OLMESARTAN MEDOXOMIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211049
Product Number: 003
Approval Date: Feb 22, 2019
Applicant Holder Full Name: SUNSHINE LAKE PHARMA CO LTD
Marketing Status: Prescription
Patent and Exclusivity Information