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PANTOPRAZOLE SODIUM

NDC 72865-230, PANTOPRAZOLE, tablet, delayed release, from XLCare Pharmaceuticals Inc..

Product NDC
72865-230
Status
Listed
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202882
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72865-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM40 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
72865-230-10728650230101000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)
72865-230-907286502309090 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/17468dbf-84b6-4c53-9ad5-341350d2cfab

Use it

Look up 72865-230 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72865-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72865-230. 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.