# ESOMEPRAZOLE MAGNESIUM

NDC: 16571-880
Generic name: ESOMEPRAZOLE MAGNESIUM
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20221201

FDA application: ANDA216349

## Active ingredients

- ESOMEPRAZOLE MAGNESIUM: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-880"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-880
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07ba5747-702f-47fc-9d80-5a70296b64bf