# Omeprazole Magnesium

NDC: 0363-0042
Generic name: Omeprazole Magnesium
Labeler / Manufacturer: Walgreens Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20150901

FDA application: ANDA078878

## 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:"0363-0042"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-0042
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee8b1740-9bcf-5b70-bd8d-97f98303dc72