# omeprazole and sodium bicarbonate

NDC: 41250-938
Generic name: Omeprazole, sodium bicarbonate
Labeler / Manufacturer: Meijer Distribution Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, GELATIN COATED
Routes: ORAL
Marketing started: 20200403

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:"41250-938"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41250-938
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb7c1c5d-b915-42f5-a5a2-5f61b088028d