# Esomeprazole Magnesium

NDC: 72789-352
Generic name: Esomeprazole Magnesium
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, DELAYED RELEASE
Routes: ORAL
Marketing started: 20160421

FDA application: ANDA205606

## Active ingredients

- ESOMEPRAZOLE MAGNESIUM DIHYDRATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-352"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-352
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ac12cd05-10cf-4694-a9e8-e5f04fe162a7