Active Ingredient: OMEPRAZOLE; SODIUM BICARBONATE
Proprietary Name: OMEPRAZOLE AND SODIUM BICARBONATE
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 20MG/PACKET;1.68GM/PACKET
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A079182
Product Number: 001
Approval Date: Apr 19, 2013
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: OMEPRAZOLE; SODIUM BICARBONATE
Proprietary Name: OMEPRAZOLE AND SODIUM BICARBONATE
Dosage Form; Route of Administration: FOR SUSPENSION; ORAL
Strength: 40MG/PACKET;1.68GM/PACKET
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A079182
Product Number: 002
Approval Date: Apr 19, 2013
Applicant Holder Full Name: STRIDES PHARMA GLOBAL PTE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information