# Omeprazole

NDC: 58602-837
Generic name: Omeprazole
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20230428

FDA application: ANDA213201

## Active ingredients

- OMEPRAZOLE MAGNESIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58602-837"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-837
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19097902-a5e6-423a-8569-31c569cd3cdb