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: A204922
Product Number: 001
Approval Date: Aug 19, 2016
Applicant Holder Full Name: AUROLIFE PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information