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Esomeprazole Magnesium

NDC 72789-352, Esomeprazole Magnesium, capsule, delayed release, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-352
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205606
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-352 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ESOMEPRAZOLE MAGNESIUM DIHYDRATE20 mg/1

Pharmacologic classes

Cytochrome P450 2C19 Inhibitors [MoA]; Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
72789-352-307278903523030 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-352-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac12cd05-10cf-4694-a9e8-e5f04fe162a7

Use it

Look up 72789-352 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-352 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-352. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.