Active Ingredient: OMEPRAZOLE; SODIUM BICARBONATE
Proprietary Name: OMEPRAZOLE AND SODIUM BICARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 20MG;1.1GM
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207476
Product Number: 001
Approval Date: Dec 6, 2016
Applicant Holder Full Name: SCIEGEN PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: OMEPRAZOLE; SODIUM BICARBONATE
Proprietary Name: OMEPRAZOLE AND SODIUM BICARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 40MG;1.1GM
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A207476
Product Number: 002
Approval Date: Dec 6, 2016
Applicant Holder Full Name: SCIEGEN PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information