# Omeprazole and Sodium Bicarbonate

NDC: 70954-797
Generic name: Omeprazole and Sodium Bicarbonate
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20260115

FDA application: ANDA219161

## Active ingredients

- OMEPRAZOLE: 20 mg/1
- SODIUM BICARBONATE: 1680 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-797"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-797
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63c3bd6c-a586-4ec0-8f45-ed936936dfeb