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PANTOPRAZOLE SODIUM

NDC 72189-112, pantoprazole, tablet, delayed release, from DIRECT RX.

Product NDC
72189-112
Status
Listed
Labeler
DIRECT RX
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/72189-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72189-112-307218901123030 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-30)
72189-112-607218901126060 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-60)
72189-112-907218901129090 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a7e7c1ab-3e75-1ff8-e053-2995a90a7539

Use it

Look up 72189-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-112. 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.