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RABEPRAZOLE SODIUM

NDC 72189-169, RABEPRAZOLE SODIUM, tablet, delayed release, from DIRECT RX.

Product NDC
72189-169
Status
Listed
Labeler
DIRECT RX
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208644
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RABEPRAZOLE SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72189-169-307218901693030 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-30)
72189-169-607218901696060 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-60)
72189-169-907218901699090 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b1b7def0-834f-37f5-e053-2a95a90ade1f

Use it

Look up 72189-169 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-169 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-169. 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.