# Omeprazole and sodium bicarbonate

NDC: 0363-0732
Generic name: Omeprazole, sodium bicarbonate
Labeler / Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 20160715

FDA application: ANDA201361

## Active ingredients

- OMEPRAZOLE: 20 mg/1
- SODIUM BICARBONATE: 1100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0363-0732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-0732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8753a131-f8b1-48e1-993b-73c1ee635fef