# omeprazole

NDC: 57483-740
Generic name: omeprazole
Labeler / Manufacturer: INNOVUS PHARMACEUTICALS, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20200806

FDA application: ANDA210593

## Active ingredients

- OMEPRAZOLE MAGNESIUM: 20.6 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57483-740"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57483-740
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce5c9fdc-0c50-4315-8f11-e00c9810abd0