# Omeprazole

NDC: 62756-377
Generic name: Omeprazole
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20190101

FDA application: ANDA207891

## Active ingredients

- OMEPRAZOLE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62756-377"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62756-377
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51c3ef34-b7c1-419e-a784-ae82540c7a22