# Omeprazole and sodium bicarbonate

NDC: 37808-732
Generic name: Omeprazole, sodium bicarbonate
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 20170825

FDA application: ANDA201361

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ddc8d73f-f4a1-42a7-89ee-420346820f61