Product Details for ANDA 207029
HYDROCORTISONE (HYDROCORTISONE)
5MG
Marketing Status: Prescription
10MG
Marketing Status: Prescription
20MG
Marketing Status: Prescription
5MG
Marketing Status: Prescription
Active Ingredient: HYDROCORTISONE
Proprietary Name: HYDROCORTISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207029
Product Number: 001
Approval Date: Apr 27, 2017
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status: Prescription
Patent and Exclusivity Information
HYDROCORTISONE (HYDROCORTISONE)
Proprietary Name: HYDROCORTISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207029
Product Number: 001
Approval Date: Apr 27, 2017
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status: Prescription
Patent and Exclusivity Information
10MG
Marketing Status: Prescription
Active Ingredient: HYDROCORTISONE
Proprietary Name: HYDROCORTISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207029
Product Number: 002
Approval Date: Apr 27, 2017
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status: Prescription
Patent and Exclusivity Information
HYDROCORTISONE (HYDROCORTISONE)
Proprietary Name: HYDROCORTISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207029
Product Number: 002
Approval Date: Apr 27, 2017
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status: Prescription
Patent and Exclusivity Information
20MG
Marketing Status: Prescription
Active Ingredient: HYDROCORTISONE
Proprietary Name: HYDROCORTISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207029
Product Number: 003
Approval Date: Apr 27, 2017
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status: Prescription
Patent and Exclusivity Information
Proprietary Name: HYDROCORTISONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207029
Product Number: 003
Approval Date: Apr 27, 2017
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status: Prescription
Patent and Exclusivity Information