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Pantoprazole Sodium

NDC 87441-065, Pantoprazole Sodium, tablet, delayed release, from Unit Dose Solutions, Inc..

Product NDC
87441-065
Status
Listed
Labeler
Unit Dose Solutions, Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202038
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87441-065 \
  -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
87441-065-018744100650130 TABLET, DELAYED RELEASE in 1 BLISTER PACK (87441-065-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5566b4b1-b4f5-4020-e063-6394a90a5257

Use it

Look up 87441-065 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87441-065 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87441-065. 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.